Category Pharma/Biotech

Enanta Pharmaceuticals Announces Fiscal First Quarter Financial Results for December 31, 2023, Hosting Webcast and Conference Call Today at 4:30 p.m. ET

Enanta Pharmaceuticals, Inc. (NASDAQ: ENTA), a clinical-stage biotechnology firm specializing in small molecule drugs within virology and immunology, has released its financial results for the fiscal first quarter ending December…

Read MoreEnanta Pharmaceuticals Announces Fiscal First Quarter Financial Results for December 31, 2023, Hosting Webcast and Conference Call Today at 4:30 p.m. ET

Longboard Pharmaceuticals Discloses Inducement Grants in Accordance with Nasdaq Listing Rule 5635(C)(4)

Longboard Pharmaceuticals, a clinical-stage biopharmaceutical company dedicated to pioneering transformative medicines for neurological diseases, has officially granted inducement awards to five new employees. The Compensation Committee of the Board of…

Read MoreLongboard Pharmaceuticals Discloses Inducement Grants in Accordance with Nasdaq Listing Rule 5635(C)(4)

Napp Secures Approval for REZZAYO® from the UK Medicines and Healthcare Products Regulatory Agency for Treating Invasive Candidiasis in Adults.

For Exclusive Distribution to GB Trade and Medical Media REZZAYO® (rezafungin) is approved for treating invasive candidiasis in adults. Adherence to official guidelines regarding the appropriate use of antifungal agents…

Read MoreNapp Secures Approval for REZZAYO® from the UK Medicines and Healthcare Products Regulatory Agency for Treating Invasive Candidiasis in Adults.

Navidea Biopharmaceuticals, Inc. Files Form 15 to Voluntarily Deregister and Suspend its SEC Reporting Obligations

Navidea Biopharmaceuticals, Inc. announced today the filing of Form 15 to voluntarily deregister and suspend SEC reporting obligations. The company maintains strategic focus on its Fix, Fund, Propel approach. Navidea…

Read MoreNavidea Biopharmaceuticals, Inc. Files Form 15 to Voluntarily Deregister and Suspend its SEC Reporting Obligations

Sensorion Receives Authorization to Initiate a Phase 1/2 Clinical Trial for SENS-501 (OTOF-GT), its Most Advanced Gene Therapy Candidate, in Select European Countries

a pioneering clinical-stage biotechnology company specializing in the development of novel therapies to restore, treat and prevent hearing loss disorders, today announces that it has received approval of its application…

Read MoreSensorion Receives Authorization to Initiate a Phase 1/2 Clinical Trial for SENS-501 (OTOF-GT), its Most Advanced Gene Therapy Candidate, in Select European Countries

FDA Approves Merck’s KEYTRUDA® (pembrolizumab) Plus Chemoradiotherapy as Treatment for Patients With FIGO 2014 Stage III-IVA Cervical Cancer

KEYTRUDA is the first and only anti-PD-1 therapy approved in combination with chemoradiotherapy for these patients Approval marks third FDA-approved indication for KEYTRUDA in cervical cancer and 39th indication for KEYTRUDA…

Read MoreFDA Approves Merck’s KEYTRUDA® (pembrolizumab) Plus Chemoradiotherapy as Treatment for Patients With FIGO 2014 Stage III-IVA Cervical Cancer