Newsroom

April 12, 2018

ERYTECH to Present Results from Phase I Trial of eryaspase in ALL and New Pre-clinical Data at AACR 2018

Lyon (France), April 12, 2018 – ERYTECH Pharma (Euronext Paris: ERYP - Nasdaq: ERYP), a clinical-stage biopharmaceutical company developing innovative therapies by encapsulating therapeutic drug substances inside red blood cells, today announced that it will present full results from its U.S. Phase I trial evaluating eryaspase (GRASPA) in combination with chemotherapy for the treatment of acute lymphoblastic leukemia (ALL) and pre-clinical data on the erymethionase program at the upcoming American Association for Cancer Research Annual Meeting, being held April 14-18, 2018 in Chicago, Illinois.
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March 13, 2018

ERYTECH to Webcast Presentation at the Cowen and Company 38th Annual Healthcare Conference

ERYTECH Pharma (Euronext Paris: ERYP - Nasdaq: ERYP), a clinical-stage biopharmaceutical company developing innovative therapies by encapsulating therapeutic drug substances inside red blood cells, today announced that Chief Executive Officer, Gil Beyen, will present at the Cowen and Company 38th Annual Health Care Conference on Wednesday, March 14, 2018 at The Marriott Copley Place, in Boston, MA.
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March 12, 2018

ERYTECH Provides Business Update and Reports Financial Results for Full Year 2017

ERYTECH Pharma (Euronext: ERYP - Nasdaq: ERYP), a clinical-stage biopharmaceutical company developing innovative therapies by encapsulating therapeutic drug substances inside red blood cells, today provided a business update and reported its financial results for the year ended December 31, 2017.
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March 6, 2018

ERYTECH to Host Fourth Quarter and Full Year 2017 Conference Call and Business Update

ERYTECH Pharma (Euronext Paris: ERYP - Nasdaq: ERYP), a clinical-stage biopharmaceutical company developing innovative therapies by encapsulating therapeutic drug substances inside red blood cells, today announced that it will host its fourth quarter and full year 2017 conference call and webcast on Tuesday, March 13, 2018, at 1:30 PM CET/8:30 AM EST to discuss operational highlights.
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February 13, 2018

ERYTECH Selects Triple Negative Breast Cancer as Next Indication for Eryaspase

LYON, France – February 13, 2018 - ERYTECH Pharma (Euronext Paris: ERYP - Nasdaq: ERYP), a clinical-stage biopharmaceutical company developing innovative therapies by encapsulating therapeutic drug substances inside red blood cells, today announced the selection of Triple Negative Breast Cancer as the next target indication for broadening the scope of eryaspase (GRASPA®) development in solid tumors.
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February 8, 2018

ERYTECH to Present at the 2018 BIO CEO & Investor Conference

LYON, France – February 8, 2018 - ERYTECH Pharma (Euronext Paris: ERYP, Nasdaq: ERYP), a clinical-stage biopharmaceutical company developing innovative therapies by encapsulating therapeutic drug substances inside red blood cells, today announced that Gil Beyen, Chief Executive Officer, will present at the 2018 BIO CEO & Investor Conference, being held February 12-13, 2018 at the New York Marriott Marquis in New York City.
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January 31, 2018

Monthly information related to total number of voting rights and shares composing the share capital

Article 223-16 of general regulation of French Autorité des Marchés Financiers Lyon - France
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December 8, 2017

ERYTECH Reports Top-line Results of Phase 2b Study of Eryaspase for the Treatment of AML

ERYTECH Pharma (Euronext Paris: ERYP) (Nasdaq: ERYP) ("ERYTECH"), a clinical-stage biopharmaceutical company developing innovative therapies by encapsulating therapeutic drug substances inside red blood cells, today announced topline results from its Phase 2b clinical study evaluating eryaspase (GRASPA®) for the treatment of acute myeloid leukemia (AML).
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November 15, 2017

ERYTECH Announces Commencement of Trading of ADSs on Nasdaq and Full Exercise of Underwriters’ Option, Bringing Gross Proceeds of Global Offering to $144 Million

ERYTECH Pharma today announced the initial closing of its previously announced global offering to specified categories of investors of an aggregate of 5,374,033 new ordinary shares, comprising an offer of 4,686,106 ordinary shares in the form of American Depositary Shares, each representing one ordinary share ("ADSs"), in the United States at an offering price of $23.26 per ADS and a concurrent private placement in Europe (including France) and other countries outside of the United States and Canada of 687,927 ordinary shares at an offering price of €20.00 per ordinary share. In addition, the underwriters for the global offering have exercised in full their option to purchase at the same price 702,915 additional ADSs and 103,189 additional ordinary shares in the global offering, with the additional closing expected to occur on November 16, 2017. Following the additional closing, aggregate net proceeds to ERYTECH, after deducting underwriting commissions and estimated offering expenses payable by ERYTECH, will be approximately $130 million. All of the securities sold in the global offering were offered by ERYTECH.
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November 14, 2017

ERYTECH to Webcast Presentation at Jefferies 2017 London Healthcare Conference

ERYTECH Pharma today announced that Gil Beyen, Chairman and Chief Executive Officer, will present at the Jefferies Global Healthcare on November 15th, 2017 at the Waldorf Hilton Hotel (Aldwych) in London, UK.
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November 13, 2017

ERYTECH to Host Third Quarter 2017 Conference Call and Business Update on November 14, 2017

ERYTECH Pharma today announced that it will host a Third Quarter 2017 conference call and webcast on Tuesday, November 14, 2017, at 2:30 PM CET/8:30 AM EST to discuss operational highlights.
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November 10, 2017

Erytech announces trading resumption of its ordinary shares on Euronext Paris

ERYTECH Pharma announces trading resumption of its ordinary shares on Euronext Paris as from 4:00pm CET.
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November 10, 2017

ERYTECH Announces Pricing of Global Offering and Approval to List on Nasdaq Global Select Market

ERYTECH Pharma today announced the pricing of its global offering to specified categories of investors of an aggregate of 5,374,033 new ordinary shares, comprising an offer of 4,686,106 ordinary shares in the form of American Depositary Shares, each representing one ordinary share ("ADSs"), in the United States at an offering price of $23.26 per ADS and a concurrent private placement in Europe (including France) and other countries outside of the United States and Canada of 687,927 ordinary shares at the corresponding offering price of €20 per ordinary share (together, the "Global Offering"), for aggregate gross proceeds of approximately $125 million before deducting underwriting commissions and estimated expenses payable by the Company. In addition, ERYTECH has granted the underwriters a 30-day option to purchase up to 806,104 additional ADSs and/or ordinary shares on the same terms and conditions, representing 15% of the ADSs and/or ordinary shares to be issued by the Company in the Global Offering (the "Over-allotment Option").
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November 10, 2017

Erytech announces trading suspension of its ordinary shares on Euronext Paris

Trading in the ordinary shares of ERYTECH Pharma, was suspended at the request of the Company on November 10, 2017 from 9:00 am CET in connection with its previously announced global offering in order to allow for the confirmation of allocations to investors and for the commencement of trading of the Company’s American Depositary Shares (“ADSs”) on the Nasdaq Global Select Market.
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November 6, 2017

ERYTECH Reports Third Quarter 2017 Financial Results and Provides Business Update

ERYTECH today provided a business update and reported its financial results for the quarter ended September 30, 2017.
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November 6, 2017

ERYTECH Announces Launch of Proposed Global Offering and NASDAQ Listing

ERYTECH today announced its intention to issue and sell, subject to market and other conditions, approximately $125 million corresponding to an aggregate of up to 5,319,148 of its ordinary shares in a global offering to specified categories of investors, including an offer of American Depositary Shares, each representing one ordinary share ("ADSs"), in the United States and a concurrent private placement of ordinary shares in Europe (including France) and other countries outside of the United States and Canada (together, the "Global Offering"). ERYTECH intends to grant the underwriters a 30-day over-allotment option to purchase additional ADSs and/or ordinary shares in an aggregate amount of up to 15% of the total number of ADSs and ordinary shares proposed to be sold in the Global Offering.
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October 10, 2017

ERYTECH Announces Resubmission of European Marketing Authorization Application for GRASPA in Acute Lymphoblastic Leukemia

ERYTECH today announced that it has resubmitted to the European Medicine Agency (EMA) its Marketing Authorization Application (MAA) for eryaspase (GRASPA®) for the treatment of patients with relapsed or refractory (R/R) acute lymphoblastic leukemia (ALL). The MAA resubmission includes the data from ERYTECH’s GRASPALL 2009-06 Phase 2/3 clinical trial in children and adults with R/R ALL as well as additional data to address the outstanding questions of the Committee for Medicinal Products for Human Use (CHMP) of the EMA.
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October 6, 2017

ERYTECH Files Registration Statement for Proposed Initial Public Offering in the United States

ERYTECH today announced that it has filed a registration statement on Form F-1 with the U.S. Securities and Exchange Commission (“SEC”) relating to a proposed initial public offering of its American Depositary Shares (“ADSs”), each representing one ordinary share, in the United States and a concurrent private placement of its ordinary shares in Europe and other countries outside of the United States and Canada (together, the “Global Offering”). All securities to be sold in the Global Offering will be offered by ERYTECH. The number of securities to be sold and the price range for the proposed Global Offering have not yet been determined. ERYTECH has applied to list its ADSs on the NASDAQ Global Market under the ticker symbol “ERYP.” The ordinary shares are listed on Euronext Paris under the symbol “ERYP.”
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September 28, 2017

ERYTECH Reports Determination of the Recommended Pivotal Phase 3 Dose of eryaspase in its U.S. Phase 1 Study in First Line Adult ALL

ERYTECH today announced the determination of the recommended pivotal Phase 3 dosing from its U.S. Phase 1 dose escalation study with eryaspase (GRASPA®) in first line treatment of adult ALL patients.
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September 12, 2017

ERYTECH to Present at Morgan Stanley Global Healthcare Conference

ERYTECH today announced that Gil Beyen, Chairman and Chief Executive Officer, will present at the 15th Annual Morgan Stanley Global Healthcare Conference on September 13th, 2017 at the Grand Hyatt Hotel in New York City..
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September 11, 2017

ERYTECH Reports First Half 2017 Financial Results and Provides Business Update

ERYTECH today provided a business update and reported its financial results for the six-month period ended June 30, 2017.
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September 8, 2017

ERYTECH Announces Positive Full Results from Phase 2b Study of Eryaspase in Combination with Chemotherapy for Treatment of Metastatic Pancreatic Cancer in Second-Line

ERYTECH today announced the presentation of the full data from its Phase 2b study evaluating eryaspase (GRASPA®) in combination with chemotherapy for the treatment of metastatic pancreatic cancer. The open-label, multi-center, randomized Phase 2b clinical study met its co-primary endpoints and demonstrated significant improvement in both overall survival (OS) and progression-free survival (PFS). The results will be presented during the European Society for Medical Oncology (ESMO) Annual Meeting in Madrid.

Link to Poster

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September 6, 2017

ERYTECH to Host Second Quarter 2017 Conference Call and Business Update

ERYTECH today announced that it will host a Second Quarter 2017 conference call and webcast on Tuesday, September 12, 2017, at 2:30 PM CET/8:30 AM EST to discuss operational highlights.

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September 1, 2017

ERYTECH to Present Pre-Clinical Data at the 13th International Congress of Inborn Errors of Metabolism

ERYTECH today announced that two abstracts on its preclinical erymethionase and eryminase programs were accepted for poster presentation at the 13th International Congress of Inborn Errors of Metabolism (ICIEM), being held September 5 – 8, 2017 in Rio De Janeiro, Brazil.

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August 31, 2017

ERYTECH to Present Full Results for Phase 2b Trial of eryaspase in Pancreatic Cancer at ESMO 2017

ERYTECH today announced that it will present the full data from its Phase 2b trial evaluating eryaspase for the treatment of metastatic pancreatic cancer at the upcoming European Society for Medical Oncology Annual Meeting, being held September 8 – 12, 2017 in Madrid, Spain.

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July 12, 2017

ERYTECH Announces Collaboration with Queen’s University to Advance its Product Candidate for Rare Metabolic Disorders

ERYTECH today announced that it has entered into a research collaboration with Queen’s University in Canada to advance the preclinical development of ERYTECH’s eryminase program specifically for the treatment of arginase-1 deficiency, a rare and severe metabolic disorder related to arginine metabolism. The collaboration will leverage the expertise of Queen’s University and ERYTECH’s ERYCAPS platform technology with the goal of generating in vivo proof-of-concept data in an arginase-1 deficiency animal model.

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June 6, 2017

ERYTECH PHARMA : ANNUAL GENERAL MEETING OF JUNE 27, 2017

ERYTECH announced today the modalities for making available the documents for the Annual General Meeting of June 27, 2017.

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May 18, 2017

ERYTECH Provides Business Update and Financial Highlights for Q1 2017

ERYTECH today provided a financial and business update for the first quarter of 2017 ended March 31, 2017.

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May 17, 2017

Erytech to Hold Q1 2017 Business Update Conference Call on May 19th, 2017

ERYTECH today announced that it will release its financial results and business update for the quarter ended March 31, 2017 on Thursday, May 18, 2017 after the close of trading on the Euronext Paris.

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April 13, 2017

ERYTECH TO RAISE €70.5 MILLION IN A PRIVATE PLACEMENT TO U.S. AND EUROPEAN INVESTORS

ERYTECH announces today that, in connection with the anticipated completion of a capital increase of 3,000,000 new ordinary shares reserved, it has obtained commitments from qualified investors in the United States and in Europe to purchase ordinary shares of the Company in a private placement reserved for a specified category of investors described below (the "Reserved Offering"). Total gross proceeds from the Reserved Offering placement are expected to be €70.5 million, before deducting fees and expenses. Jefferies International Limited acted as Sole Global Coordinator and acted together with Cowen and Company, LLC and Oddo & Cie as Joint Bookrunners in the Reserved Offering.

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April 4, 2017

ERYTECH Announces Launch of Investigator-Initiated Phase 2 Study of eryaspase (GRASPA®) for ALL

ERYTECH today announced the launch of an investigator-initiated study to evaluate eryaspase, also known by the trade name GRASPA®, in patients with acute lymphoblastic leukemia (ALL). The study will take place in seven Nordic countries and be conducted in collaboration with the Nordic Society of Pediatric Hematology and Oncology (NOPHO).

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April 3, 2017

ERYTECH makes its 2016 Reference Document available

ERYTECH today announced that it had filed on March 31, 2017 with the “Autorité des Marchés Financiers (AMF)”, its 2016 Reference Document, including the management report and the annual financial report.

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March 27, 2017

ERYTECH reports positive Phase 2b data for eryaspase for the treatment of metastatic pancreatic cancer

ERYTECH today announced positive topline results from its Phase 2b clinical study evaluating its product candidate, eryaspase (GRASPA®), in combination with chemotherapy for the treatment of second-line metastatic pancreatic cancer. The multicenter, randomized Phase 2b study met its prespecified co-primary endpoints, and showed significant improvement in both progression-free survival (PFS) and overall survival (OS) in patients treated with eryaspase combined with chemotherapy compared to chemotherapy alone.

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March 23, 2017

ERYTECH collaborates with Fox Chase Cancer Center to advance its platform in the field of rare metabolic disorders

ERYTECH today that it has entered into a research collaboration with Fox Chase Cancer Center (FCCC) to advance the pre-clinical development of the Company’s erymethionase program for homocystinuria, a rare and severe metabolic disorder of methionine metabolism. The collaboration will leverage FCCC’s world-class expertise to generate in vivo proof-of-concept data with erymethionase in a homocystinuria animal model.

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March 20, 2017

ERYTECH Presents New Preclinical Anti-Tumor Data on erymethionase at AACR 2017

ERYTECH today announced the presentation of new anti-tumor data supporting the Company’s preclinical product erymethionase (ERY-MET) at the upcoming American Association for Cancer Research (AACR) Annual Meeting, being held April 1 – 5, 2017 in Washington, D.C.

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March 7, 2017

ERYTECH to Present Preclinical Results Supporting Immunotherapy Potential of ERYMMUNE Platform at Two Upcoming Medical Meetings

ERYTECH today announced the presentation of encouraging preclinical data supporting the Company’s ERYMMUNE program at two upcoming immunotherapy medical meetings, World ADOPT Summit 2017 and 10th Symposium of Vaccinology. The World ADOPT Summit 2017 is being held March 7-9, 2017 at the Cavendish Conference Centre in London, U.K., and the 10th Symposium of Vaccinology is being held March 20-21, 2017 at the Université Lumière Lyon II in Lyon, France. In conjunction with the Symposium of Vaccinology, ERYTECH will also share the results with the members of the French Society of Immunology.

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March 2, 2017

ERYTECH Provides Business Update and Reports Financial Results for Full Year 2016

ERYTECH today provided a business update and reported its financial results for the year ended December 31, 2016.

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February 28, 2017

ERYTECH to hold Business Update and 2016 Financial Results Conference Call on March 3rd, 2017

ERYTECH today announced that it will release its financial results and business update for the year ended December 31, 2016 on Thursday, March 02, 2017 after the close of trading on the Euronext Paris.

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January 17, 2017

ERYTECH Presents New Preclinical Data on ERY-MET at the 2017 ASCO GI Symposium

ERYTECH today announced new data supporting the second Company’s product candidate ERY-MET will be presented at the 2017 Gastrointestinal Cancers Symposium co-sponsored by the American Society of Clinical Oncology (ASCO GI), being held January 19 – 21, 2017 in San Francisco, California.

Link to poster

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December 8, 2016

ERYTECH RAISES €10 MILLION IN PRIVATE PLACEMENT WITH U.S. AND EUROPEAN INVESTORS

ERYTECH today announced the closing of a private placement of 793,877 ordinary shares to qualified investors in the United States and Europe for total gross proceeds of approximately €10 million.

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December 1, 2016

ERYTECH Presents New Data on GRASPA’s Mechanism of Action at ASH Annual Meeting

ERYTECH today announced the presentation of promising preliminary data for the Company's lead product candidate, eryaspase, also known as ERY-ASP or under the trade name GRASPA®, at the 58th American Society of Hematology (ASH) Annual Meeting and Exposition, being held December 3-6, 2016 in San Diego, California.

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November 14, 2016

ERYTECH Announces Withdrawal of its European Marketing Authorization Application for GRASPA for Acute Lymphoblastic Leukemia and Prepares for Resubmission

ERYTECH today announced its decision to withdraw the current MAA for GRASPA for the treatment of acute lymphoblastic leukemia (ALL). The Company determined that the time allowed in the CHMP procedure was not sufficient to provide the additional data requested in the CHMP’s Day 180 List of Outstanding Issues (LOI). The Company intends to resubmit an MAA around mid-2017.

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November 3, 2016

ERYTECH Provides Business Update and Reports Financial Highlights for Third Quarter 2016

ERYTECH today provided a business update and reported its financial results for the quarter ended September 30, 2016.

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October 27, 2016

ERYTECH Strengthens Executive Leadership Team with Appointments of Chief Scientific Officer and Chief Business Officer

ERYTECH today announced the appointments of Dr. Alexander Scheer, Ph.D. as the company’s Chief Scientific Officer and Jean-Sébastien Cleiftie, as Chief Business Officer.

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October 26, 2016

ERYTECH to Hold Q3 2016 Business Update Conference Call on November 4th, 2016

ERYTECH today announced that it will release its financial results and business update for the quarter ended September 30, 2016 on Thursday, November 03, 2016 after the close of trading on the Euronext Paris.

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September 26, 2016

ERYTECH Completes Patient Enrollment in Phase 2 Trial of eryaspase (GRASPA®) for Pancreatic Cancer

ERYTECH Pharma today announced the final patient has been enrolled in its Phase 2 trial of eryaspase, also known as ERY-ASP or GRASPA®, for the treatment of pancreatic cancer.

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September 6, 2016

ERYTECH Reports Business and Financial Update for the First Half of 2016

ERYTECH Pharma today provided a business update and reported its financial results for the six month period ended June 30, 2016.

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September 5, 2016

ERYTECH Appoints Allene M. Diaz to its Board of Directors

ERYTECH Pharma today announced the appointment of Allene M. Diaz to its Board of Directors as a nonvoting member (censeur).

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August 30, 2016

ERYTECH to Hold Q2 2016 Business Update Conference Call on September 7th, 2016

ERYTECH Pharma today announced that it will release its financial results and business update for the quarter ended June 30, 2016 on Tuesday, September 06, 2016 after the close of trading on the Euronext Paris.

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August 29, 2016

ERYTECH Completes Patient Enrollment in Phase 2b Trial for eryaspase (GRASPA®) in Acute Myeloid Leukemia

ERYTECH Pharma today announced that it has reached full patient enrollment in the Phase 2b trial of eryaspase, also known as ERY-ASP or GRASPA®, for the treatment of acute myeloid leukemia (AML).

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June 3, 2016

ERYTECH PHARMA : ANNUAL GENERAL MEETING OF JUNE 24, 2016

Erytech announced today the modalities for making available the documents for the Annual General Meeting of June 24, 2016.

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May 10, 2016

ERYTECH Provides Business and Financial Highlights for First Quarter 2016

Erytech today provided a business update and reported financial results for its first quarter ended March 31, 2016.

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May 2, 2016

Erytech to Hold Q1 2016 Business Update Conference Call on May 11th, 2016

Erytech today announced that it will release its financial results and business update for the quarter ended March 31, 2016 on Tuesday, May 10, 2016 after the close of trading on the Euronext Paris.

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April 30, 2016

ERYTECH makes its 2015 Reference Document available

ERYTECH today announced that it had filed on April 29, 2016 with the “Autorité des Marchés Financiers (AMF)”, its 2015 Reference Document, including the management report and the annual financial report.

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March 17, 2016

ERYTECH to Present Two Posters at AACR

ERYTECH today announced that it will present two posters at the upcoming American Association for Cancer Research (AACR) Annual Meeting, being held April 16-20, 2016 in New Orleans, LA, USA.

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March 15, 2016

ERYTECH Receives USPTO Notice of Allowance for Patent Covering ERYCAPS Immunotherapy Technology

ERYTECH today announced that it has received a Notice of Allowance from the U.S. Patent and Trademark Office (USPTO) for U.S. Patent Application No. 12/672,094 entitled “Composition and Therapeutic Anti-tumor Vaccine.”

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February 23, 2016

ERYTECH Provides Business Update and Reports Financial Results for Full Year 2015

Conference call and webcast on Wednesday, February 24th at 15:00 pm CET/09:00 am EST

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February 18, 2016

Erytech to Hold Full-year 2015 Business Update Conference Call on February 24, 2016

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February 8, 2016

Erytech Announces 2016 Financial Calendar

ERYTECH today published its financial calendar for 2016.

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February 3, 2016

Erytech to Present at Upcoming Investor Conferences

ERYTECH will present at the 18th Annual BIO CEO and Investor Conference being held February 8-9, 2016 and the Leerink Partners 5th Annual Global Healthcare Conference being held February 10-11, 2016. Both conferences are being held at the Waldorf Astoria Hotel in New York.

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January 11, 2016

ERYTECH Reports Financial Highlights for Q4 2015

ERYTECH reports revenue and cash balance for the fourth quarter of 2015.

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January 6, 2016

ERYTECH Announces Third DSMB Safety Review and Continuation of Its Phase 2b Study in Acute Myeloid Leukemia

ERYTECH announces that an independent Data and Safety Monitoring Board (DSMB1) completed its third safety assessment of the company’s Phase 2b ENFORCE 1 study in acute myeloid leukemia (AML) and that enrollment will continue until completion.

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January 4, 2016

ERYTECH Announces Management Change

ERYTECH today announced that Yann Godfrin will be leaving the company to pursue new entrepreneurial projects.

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December 10, 2015

ERYTECH wins the European Small and Mid-Cap Award in the Most Innovative Newcomer category

ERYTECH announced today that it received yesterday evening the “European Small and Mid-Cap” award in the “Most Innovative Newcomer” category by the Federation of European Stock Exchanges.

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December 8, 2015

ERYTECH Announces Presentation of Additional Data at the American Society of Hematology 57th Annual Meeting

ERYTECH announces that investigators presented additional results from the pivotal Phase 2/3 clinical trial with GRASPA that add to the body of data supporting the potential benefit of GRASPA in combination with chemotherapy in the treatment of Acute Lymphoblastic Leukemia (ALL).

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December 7, 2015

ERYTECH raises approximately €25.4 million in a private placement

ERYTECH today announces the closing of a private placement of 940,000 ordinary shares to qualified investors in the United States and Europe for a total amount of approximately €25.4 million.

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December 3, 2015

ERYTECH to raise approximately € 25.4 million in a private placement of ordinary shares to European and U.S. institutional investors

ERYTECH today announces the pricing of a private placement of 940,000 ordinary shares to qualified investors in the United States and Europe for a total amount subscribed of approximately € 25.4 million. This private placement was conducted by Jefferies International Limited, Leerink Partners LLC and Bryan Garnier & Co. Limited, acting as placement agents and LifeSci Capital LLC, acting as co-manager.


November 18, 2015

ERYTECH wins Deloitte Technology Fast 50 “Promising Biotech Award” for France’s Grand Rhone-Alpes Region

ERYTECH announced today that it received Deloitte Technology Fast 50 award in the “Promising Biotech” category for France’s Grand Rhone-Alpes region.

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November 5, 2015

ERYTECH announces data presentations at the American Society of Hematology 57th Annual Meeting

ERYTECH announces the upcoming presentation of three abstracts at the American Society of Hematology (ASH) Annual Meeting taking place in Orlando, Florida, USA from December 5-8, 2015.

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November 3, 2015

ERYTECH reports financial highlights for Q3 2015

ERYTECH reports cash balance and revenues for the third quarter of 2015.

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October 20, 2015

ERYTECH announces publication of two articles describing clinical results with eryaspase/GRASPA

ERYTECH announces the publication of two peer-reviewed manuscripts describing clinical results obtained with eryaspase/GRASPA®.

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September 28, 2015

ERYTECH provides business update and financial results for the first half of 2015

ERYTECH provides a business update and reports its financial results for the six-month period ending June 30, 2015.

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September 23, 2015

ERYTECH strengthens its intellectual property position with the issuance of United States patent for erythrocytes containing arginine deiminase

ERYTECH announces the issuance of a new patent in the United States.

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September 22, 2015

ERYTECH to host a webcast on September 29, 2015 for its 2015 half-year results

ERYTECH will announce its half-year results for 2015 on Monday September 28, 2015, after market close, and hold a presentation webcast on the September 29, 2015 at 2:30 pm CET / 8:30 am EDT.

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September 14, 2015

ERYTECH submits EMA Marketing Authorization Application for GRASPA to treat acute lymphoblastic leukemia

ERYTECH announces today the submission of a centralized Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) for eryaspase (Invented Name: GRASPA®) for the treatment of patients with acute lymphoblastic leukemia (ALL).

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September 1, 2015

ERYTECH appoints Eric Soyer as Chief Financial and Chief Operating Officer

ERYTECH announces the appointment of Eric Soyer as Chief Financial and Chief Operating Officer (CFO/COO).

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July 28, 2015

ERYTECH announces plans to conduct registered initial public offering in the United States

ERYTECH today announced that the Company plans to conduct a registered initial public offering in the United States.

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July 20, 2015

ERYTECH announces positive safety review for eryaspase in its Phase 2 study in pancreatic cancer

ERYTECH announces a positive DSMB safety review following the treatment of the first twenty-four patients with eryaspase in its Phase 2 study in pancreatic cancer.

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July 15, 2015

ERYTECH appoints Dr. Iman El-Hariry as Chief Medical Officer

ERYTECH announces the appointment of Iman El-Hariry as Chief Medical Officer, responsible for global medical, clinical and regulatory affairs.

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July 8, 2015

ERYTECH reports financial highlights for Q2 2015

ERYTECH reports cash balance and revenues for the second quarter of 2015.

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June 22, 2015

ERYTECH announces two positive DSMB reviews

ERYTECH announces positive safety reviews after the completion of the first cohort in the company’s US Phase I study with eryaspase in Acute Lymphoblastic Leukemia (ALL), and following the treatment of the first three patients with eryaspase in combination with Folfox in its Phase II study in pancreatic cancer.

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June 2, 2015

ERYTECH announces presentation and webcast at the Jefferies 2015 Healthcare Conference

ERYTECH announces that Gil Beyen, Chairman & CEO of the company, will present a company overview at the Jefferies 2015 HealthCare Conference in New York on June 4 at 9:00 am Eastern Time.

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June 1, 2015

ERYTECH reported full GRASPA® Phase III results in ALL and provided update on AML Phase IIb at ASCO

ERYTECH reported complete Phase III results of its pivotal program with GRASPA® in Acute Lymphoblastic Leukemia (ALL) and presented the design of the ongoing Phase IIb study in Acute Myeloid Leukemia (AML) at the 51st Annual Meeting of the American Society of Clinical Oncology (ASCO). During an investigator meeting ERYTECH also presented the progress and plans on other development programs.

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May 20, 2015

ERYTECH announces oral presentations of GRASPA® Phase III results at ASCO and EHA annual meetings

ERYTECH announces that the data related to GRASPA® Phase 3 pivotal program in Acute Lymphoblastic Leukemia (ALL) will be the subject of oral presentations at the 51st Annual Meeting of the American Society of Clinical Oncology (ASCO), May 29 - June 2, Chicago, USA, and at the 20th Congress of European Hematology, June 11 - 14, Vienna, Austria. A poster on the design of the ongoing Phase IIb study in Acute Myeloid Leukemia (AML) will also be presented at ASCO.

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May 5, 2015

ERYTECH reports financial highlights for Q1 2015

ERYTECH reports cash balance and revenues for the first quarter of 2015.

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May 5, 2015

ERYTECH announces positive DSMB annual review of its Expanded Access Program in ALL

ERYTECH announces that an independent Data and Safety Monitoring Board (DSMB) completed its first safety assessment of the company’s Expanded Access Program (EAP) in Acute Lymphoblastic Leukemia (ALL) and recommended continuation of the program without modification.

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April 28, 2015

ERYTECH receives the EnterNext Tech 40 Label

ERYTECH has received the EnterNext Tech 40 Label and announces its inclusion in the Tech 40 index.

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April 21, 2015

ERYTECH strengthens its intellectual property position in the US

ERYTECH announces the strengthening of its intellectual property portfolio in the United States with the granting of a new patent and the further extension of the patent term of its core process patent.

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March 30, 2015

ERYTECH provides business update and financial results for the full year 2014

ERYTECH provides a business update and reports its financial results for the period ending December 31, 2014.

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March 26, 2015

ERYTECH appoints new independent board member

ERYTECH announces it has coopted Luc Dochez as new independent board member and will propose his appointment at the upcoming general assembly in June.

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March 24, 2015

ERYTECH announces three data presentations at the 2015 AACR Annual Meeting

ERYTECH announces the upcoming presentation of three abstracts, at the American Association for Cancer Research (AACR) taking place in Philadelphia, PA, USA from 18 to 22 April 2015.

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February 10, 2015

ERYTECH reports financial highlights for Q4 2014 and updates on upcoming milestones

ERYTECH reports revenues and cash balance for the fourth quarter of 2014 and provides an update on upcoming milestones.

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January 15, 2015

ERYTECH announces its financial calendar for 2015

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January 12, 2015

ERYTECH announces ADR Level 1 listing in the US

ERYTECH today announced the launch of a sponsored American Depository Receipt (ADR) Level 1 listing in the United States in order to support the expansion of the Company's US investor base.

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January 8, 2015

ERYTECH announces management change

ERYTECH today announced that Pierre-Olivier Goineau will be leaving the company to pursue other interests.

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December 8, 2014

ERYTECH reports additional positive Phase III results from clinical study with eryaspase/GRASPA® in Acute Lymphoblastic Leukemia

ERYTECH reports additional positive Phase III results from the pivotal study with eryaspase/GRASPA® in Acute Lymphoblastic Leukemia.

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November 14, 2014

ERYTECH to present at Jefferies Global Healthcare Conference

ERYTECH will be presenting at Jefferies Global Healthcare Conference in London next week.

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November 7, 2014

ERYTECH to report positive initial results on the use of GRASPA® in ALL patients allergic to E. Coli and Erwinia derived asparaginases at ASH

ERYTECH announces the presentation of four case studies with GRASPA® in an expanded access program at the 56th Annual Meeting of the American Society of Hematology (ASH), December 6-9, 2014, in San Francisco, CA.

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October 23, 2014

ERYTECH successfully raises €30 million for expanding its therapeutic indications in oncology and accelerating its clinical developments

ERYTECH announces today the successful completion of a capital increase for a total amount of €30 million.

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October 20, 2014

ERYTECH announces granting of new patent in the United States

ERYTECH announces the granting of a new patent in the field of asparaginase in the United States.

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October 9, 2014

ERYTECH wins EuropaBio’s Most Innovative European Biotech SME Award 2014

ERYTECH won EuropaBio’s Most Innovative European Biotech SME Award 2014.

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September 30, 2014

ERYTECH reports positive top-line Phase III results from clinical study with GRASPA® in Acute Lymphoblastic Leukemia

ERYTECH reports positive Phase III results from its pivotal study with GRASPA® in Acute Lymphoblastic Leukemia.

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September 2, 2014

ERYTECH business update and financial results for the first half of 2014

ERYTECH provides a business update and reports its financial results for the period ending June 30, 2014.

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August 27, 2014

ERYTECH announces second positive DSMB review of its Phase IIb study in Acute Myeloid Leukemia

ERYTECH announces that an independent Data and Safety Monitoring Board (DSMB) completed its second safety assessment of the company’s Phase IIb study in Acute Myeloid Leukemia (AML) and unanimously recommended continuation of the trial without modification.

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July 28, 2014

ERYTECH announces enrollment of first patient in Phase II study of eryaspase in pancreatic cancer

ERYTECH announces the enrollment of the first patient in its Phase II study with eryaspase in second line treatment of patients affected by pancreatic cancer.

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July 22, 2014

ERYTECH announces enrollment of first patient in Phase I/II study of eryaspase in Acute Lymphoblastic Leukemia in the United States

ERYTECH announces the enrollment of the first patient in its Phase I/II study with eryaspase in Acute Lymphoblastic Leukemia in the United States of America.

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July 16, 2014

ERYTECH provides financial update for Q2 2014

ERYTECH provides a financial update for the second quarter of 2014.

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June 18, 2014

ERYTECH appoints two new independent board members

ERYTECH announces it has appointed Dr Martine George and Mrs Hilde Windels as new independent members to its board of directors.

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June 2, 2014

ERYTECH strengthens its intellectual property portfolio

ERYTECH announces the granting of two key patents for its core product eryaspase.

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May 15, 2014

ERYTECH provides financial update for Q1 2014

ERYTECH provides a financial update for the first quarter of 2014.

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May 6, 2014

ERYTECH receives authorization to start its Phase II clinical study in pancreatic cancer

ERYTECH announces that the ANSM, French healthcare agency, has granted the authorization to start a Phase II study in second line treatment of patients affected by pancreatic cancer.

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April 29, 2014

ERYTECH provides business update and financial results for the full year 2013

ERYTECH provides a business update and reports its financial results for the period ending December 31, 2013.

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April 9, 2014

ERYTECH adds a new product candidate to its Cancer Metabolism development portfolio

ERYTECH announces the addition of a new product development candidate, erymethionase, to the company’s Cancer Metabolism product pipeline.

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April 2, 2014

ERYTECH receives Orphan Drug Designation by the FDA for eryaspase in Acute Myeloid Leukemia

ERYTECH announces that its lead product GRASPA®/eryasp1 has been granted Orphan Drug Designation by the U.S. Food and Drug Administration (FDA) for the treatment of Acute Myeloid Leukemia (AML), an aggressive form of blood cancer.

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February 13, 2014

ERYTECH welcomes new US and European investors

ERYTECH was informed today that certain of its historical institutional investors have sold part of their holdings to new specialized life sciences investors in the United States and in Europe.

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January 28, 2014

ERYTECH PHARMA launches a subscription of BSPCE warrants reserved for its main executives

ERYTECH launch a subscription of BSPCE reserved for its main executives.

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January 27, 2014

ERYTECH gives feedback on its first Investor R&D Day and provides a financial and business update for Q4 2013

ERYTECH held its first Investor R&D day and provides a financial and business update for the fourth quarter of 2013.

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January 20, 2014

ERYTECH announces its financial calendar for 2014

ERYTECH announces its financial calendar for 2014

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January 15, 2014

ERYTECH announces clinical trial authorizations in Finland and Spain for its European Phase IIb study in AML

ERYTECH announces it received authorizations for its Phase IIb GRASPA-ML clinical trial in Acute Myeloid Leukemia (AML) in Finland and Spain.

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January 7, 2014

ERYTECH positions its lead product in solid tumors and launches a Phase II clinical study in pancreatic cancer

ERYTECH provides an update on its development plans to broaden the scope of its lead product eryaspase into the large field of solid tumors and announces the launch of a Phase II study in pancreatic cancer.

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December 20, 2013

ERYTECH announces the decision of USPTO to extend the additional exclusivity period of its core process patent to almost 4 years

ERYTECH announces its received final notification of allowance for the granting of its core process patent in the United States in which the term of exclusivity has been further extended from two to almost four years

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December 6, 2013

ERYTECH announces two presentations at 55th ASH annual meeting and exposition in New Orleans

ERYTECH announces that data related to the Company’s lead product GRASPA® will be the subject of two poster presentations at the 55th American Society of Hematology (ASH) Annual Meeting and Exhibition on December 7 and 8 in New Orleans, USA.

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November 12, 2013

ERYTECH announces positive DSMB review of its Phase IIb study in Acute Myeloid Leukemia

ERYTECH announces that an independent Data and Safety Monitoring Board (DSMB) completed its first assessment of the company’s Phase IIb study in Acute Myeloid Leukemia (AML) study and unanimously recommended continuation of the trial without modification.

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November 5, 2013

ERYTECH provides financial update for Q3 2013

ERYTECH announces today its cash position and its revenues for the third quarter of 2013.

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September 16, 2013

ERYTECH announces the granting of its core process patent in the United States with two additional years of exclusivity

ERYTECH announces it received notification of allowance for the granting of its core process patent in the United States with two additional years of exclusivity in the United States.

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September 10, 2013

ERYTECH completes enrollment in its Phase III study in Acute Lymphoblastic Leukemia

ERYTECH announces the completion of the enrollment of patients in its pivotal Phase III study in Acute Lymphoblastic Leukemia (ALL).

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August 28, 2013

ERYTECH business update and financial results for the first half of 2013

ERYTECH provides a business update and reports its financial results for the period ending June 30, 2013.

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July 18, 2013

ERYTECH provides financial update for Q2 2013

ERYTECH announced today its cash position and its revenues for the second quarter of 2013.

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July 4, 2013

ERYTECH announces fast take-off of its Phase IIb study in Acute Myeloid Leukemia

ERYTECH announces a fast take-off of its Phase IIb study in Acute Myeloid Leukemia (AML).

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June 3, 2013

ERYTECH provides financial update for Q1 2013

ERYTECH announced today its cash position and its revenues for first quarter 2013.

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May 20, 2013

ERYTECH to present at upcoming investor conferences

ERYTECH announced today that in May and June the company will present at several visible investor events in Europe and the U.S following its successful IPO on April, 2013. As a public company ERYTECH is committed to actively engage with investors and the financial community.

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April 30, 2013

ERYTECH’s IPO a remarkable success, raising €17.7 million

ERYTECH today announced the success of its IPO in compartment C of the NYSE Euronext regulated market in Paris, raising more than the target amount of €15 million.

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April 18, 2013

ERYTECH announces its IPO on NYSE Euronext Paris regulated market

ERYTECH today announces that the French market regulator Autorité des Marchés Financiers (AMF) granted its visa n°13-166 on April 17, 2013 for the prospectus relative to the listing of ERYTECH shares on the NYSE Euronext regulated market in Paris.

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April 3, 2013

ERYTECH Pharma receives FDA IND clearance to initiate a clinical study in Acute Lymphoblastic Leukemia in the U.S.

ERYTECH announced today that it has received clearance of its Investigational New Drug (IND) Application from the United States Food and Drug Administration (FDA) to initiate a Phase I clinical trial of its product ERYASP®, L-asparaginase loaded erythrocytes, in patients 40 years or older with newly diagnosed Acute Lymphoblastic Leukemia (ALL).

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November 23, 2012

ERYTECH Pharma signs licensing and distribution agreement with Orphan Europe for GRASPA® in Europe

Erytech Pharma announced today that it has entered into a definitive agreement and Orphan Europe, part of the Recordati Group, granting Orphan Europe exclusive rights for the commercialization and distribution of GRASPA® in Acute Lymphoblastic Leukemia (ALL) and Acute Myeloid Leukemia (AML) in Europe.

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Septembre 7, 2012

ERYTECH Pharma announces the oral presentation of very demonstrative results regarding its technology to Induce specific immune tolerance by antigen loaded erythrocytes.

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June 17, 2012

ERYTECH Pharma announces the oral presentation of positive Phase II clinical trial results in Acute Lymphoblastic Leukemia.

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June 13, 2012

ERYTECH Pharma’s sickle cell treatment receives positive opinion for Orphan Drug Designation from the European Medicines Agency

Erytech Pharma announces that the Committee for Orphan Medicinal Products (COMP) of the European Medicines Agency (EMA) adopted a positive opinion to grant Orphan Drug Designation (ODD) to its investigational product ENHOXY® for sickle cell disease.

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June 5, 2012

ERYTECH PHARMA receives € 7 Million from OSEO to lead the TEDAC personalized medicine project in cancer

ERYTECH Pharma is pleased to announce that it received a total of € 6.95 million in support from the Strategic Industrial Innovation program of the French public organization OSEO to lead the TEDAC project (Therapeutic Enzymes to Deplete Amino acids to treat Cancers resistant to radio/chemotherapy).

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June 27, 2011

ERYTECH Pharma completes the enrollment of patients in its Phase I clinical trial in pancreatic cancer

ERYTECH Pharma has just completed the enrollment of patients in a Phase I clinical trial with its flagship product for pancreatic cancer, Graspa®.

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May 17, 2011

ERYTECH Pharma to partner with Teva for long term distribution agreement in Israel

ERYTECH Pharma is pleased to announce it has signed an exclusive long term agreement with Teva for the registration, marketing, distribution and sale of Graspa®, the company‟s lead product, in Israel.

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March 14, 2011

ERYTECH Pharma to present promising results for the treatment of Sickle Cell Disease

ERYTECH Pharma will in the near future present their promising results obtained with the GR-ARA1 project for the treatment of sickle cell disease.

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February 17, 2011

ERYTECH Pharma announces appointment of Marc Beer to the Supervisory Board

ERYTECH Pharma is pleased to welcome Marc Beer as a new board member.

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