WALTHAM, Mass., May 2, 2019 (ACCESSWIRE) — EyeGate Pharmaceuticals, Inc. (NASDAQ: EYEG) (“EyeGate” or “the Company”) announced today it has successfully submitted the Investigational Device Exemption (“IDE”) to the U.S. Food and Drug Administration (“FDA”) regarding its photorefractive keratectomy (“PRK”) pivotal study. The review process takes 30 days, at which point the FDA will allow…
Continued Expansion of the EyeGate OBG Franchise WALTHAM, Mass., May 30, 2018 (GLOBE NEWSWIRE) — EyeGate Pharmaceuticals, Inc. (NASDAQ:EYEG) (“EyeGate” or the “Company”), a clinical-stage, specialty pharmaceutical company with two proprietary platform technologies for treating diseases and disorders of the eye, today announced the filing of an Investigational Device Exemption (IDE) supplement for Punctate Epitheliopathy…
Top line Data expected in Q3 2018 WALTHAM, Mass., April 06, 2018 — EyeGate Pharmaceuticals, Inc. (NASDAQ:EYEG) (“EyeGate” or the “Company”), today announced completion of patient enrollment for the pivotal Phase 3 clinical study of its EGP-437 combination product for the treatment of non-infectious anterior uveitis. Non-infectious anterior uveitis is characterized by the inflammation of…
Triggers Milestone Payment under Global Licensing Agreement with Valeant Pharmaceuticals WALTHAM, Mass., Nov. 08, 2017 — EyeGate Pharmaceuticals, Inc. (NASDAQ:EYEG) (“EyeGate” or the “Company”), a clinical-stage, specialty pharmaceutical company with two platform technologies for treating diseases and disorders of the eye, has completed enrollment in the double-masked, randomized, placebo-controlled Phase 2b trial of its EGP-437…
WALTHAM, MA / ACCESSWIRE / March 26, 2019 / EyeGate Pharmaceuticals, Inc. (NASDAQ: EYEG) (“EyeGate” or “the Company”) has met with the U.S. Food and Drug Administration (“FDA”) regarding its Ocular Bandage Gel (“OBG”) product and has confirmed its path to a de novo filing. The FDA has agreed that based on the strength of…
A product marketing veteran with an ophthalmology focus at companies such as Santen, Merck and Pharmacia WALTHAM, Mass., Nov. 01, 2017 — EyeGate Pharmaceuticals, Inc. (NASDAQ:EYEG) (“EyeGate” or the “Company”), a clinical-stage, specialty pharmaceutical company with two proprietary platform technologies for treating diseases and disorders of the eye, has appointed Mike Garanzini as Chief Commercial…
Further Strengthens Global IP Protection for EGP-437 WALTHAM, Mass., Dec. 19, 2017 — EyeGate Pharmaceuticals, Inc. (NASDAQ:EYEG) (“EyeGate” or the “Company”), a clinical-stage, specialty pharmaceutical company with two platform technologies for treating diseases and disorders of the eye, today announced that it has been granted U.S. Patent No. 9,820,935, by the U.S. Patent and Trademark…
FDA Grants Approval for Studies for Patients that have undergone Photorefractive Keratectomy and for Patients with Punctate Epitheliopathies WALTHAM, Mass., July 24, 2018 – EyeGate Pharmaceuticals, Inc. (NASDAQ: EYEG) (“EyeGate” or the “Company”), a clinical-stage, specialty pharmaceutical company with two proprietary platform technologies for treating diseases and disorders of the eye, today announced the U.S.…
WALTHAM, Mass., June 26, 2019 (ACCESSWIRE) — EyeGate Pharmaceuticals, Inc. (NASDAQ: EYEG) (“EyeGate” or “the Company”) announced today it has enrolled the first patient in its corneal wound repair pivotal study in patients having undergone photorefractive keratectomy (“PRK”) surgery. Barbara Wirostko MD, Chief Medical Officer of EyeGate, said, “There is a significant need for an…
WALTHAM, Mass., Aug. 01, 2016 — EyeGate Pharmaceuticals, Inc. (NASDAQ:EYEG) (“EyeGate” or the “Company”), a specialty pharmaceutical company that focuses on developing and commercializing products for treating diseases and disorders of the eye, today announced positive data from its Phase 1b/2a trial assessing its lead product candidate, iontophoretic EGP-437, in the treatment of post-operative ocular…