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Merck Updates on Phase 3 Trial of Favezelimab-Pembrolizumab Combo in Colorectal Cancer

  • The Pharma Data
  • September 28, 2024

Merck (NYSE: MRK), known as MSD outside the U.S. and Canada, has announced that the Phase 3 KEYFORM-007 trial, which investigated the fixed-dose combination of favezelimab (Merck’s anti-LAG-3 antibody) and…

Read MoreMerck Updates on Phase 3 Trial of Favezelimab-Pembrolizumab Combo in Colorectal Cancer
  • Press Releases

BioAlberta and AxialBridge Partner to Help Alberta Life Sciences Companies Expand into the UK

  • The Pharma Data
  • September 27, 2024

BioAlberta is excited to announce a new partnership with AxialBridge as its operational and commercialization partner. This collaboration aims to assist Alberta-based biotechnology and MedTech companies in expanding their clinical…

Read MoreBioAlberta and AxialBridge Partner to Help Alberta Life Sciences Companies Expand into the UK
  • News

eClinical Solutions Pioneers the Future of Drug Development at ENGAGE 2024 Conference

  • The Pharma Data
  • September 27, 2024

eClinical Solutions LLC, a global leader in digital clinical software and services, is set to host its sixth annual client and partner conference, ENGAGE 2024, on Thursday, October 10 and…

Read MoreeClinical Solutions Pioneers the Future of Drug Development at ENGAGE 2024 Conference
  • Business

Phare Bio Secures Up to $27M from ARPA-H for AI-Driven Antibiotic Development

  • The Pharma Data
  • September 27, 2024

Phare Bio, in collaboration with the Collins Lab at the Massachusetts Institute of Technology (MIT) and Harvard’s Wyss Institute, has secured up to $27 million in funding from the Advanced…

Read MorePhare Bio Secures Up to $27M from ARPA-H for AI-Driven Antibiotic Development
  • News

BeiGene Updates on FDA Advisory Vote for PD-1 Inhibitors, Including TEVIMBRA, in ESCC and Gastric/GEJ Cancers

  • The Pharma Data
  • September 27, 2024

BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160; SSE: 688235), a global oncology company, announced that the U.S. Food and Drug Administration’s (FDA) Oncologic Drugs Advisory Committee (ODAC) has recognized the positive…

Read MoreBeiGene Updates on FDA Advisory Vote for PD-1 Inhibitors, Including TEVIMBRA, in ESCC and Gastric/GEJ Cancers
  • Regulatory

FDA Approves Bristol Myers Squibb’s COBENFY for Adult Schizophrenia Treatment

  • The Pharma Data
  • September 27, 2024

Bristol Myers Squibb (NYSE: BMY) has announced that the U.S. Food and Drug Administration (FDA) has approved COBENFY™ (xanomeline and trospium chloride), an oral medication for treating schizophrenia in adults.…

Read MoreFDA Approves Bristol Myers Squibb’s COBENFY for Adult Schizophrenia Treatment
  • News

New Study Assesses Awareness of High Breast Density as a Breast Cancer Risk Factor

  • The Pharma Data
  • September 26, 2024

In recognition of World Dense Breast Day on September 25, Bayer has announced a new study, published in Patient Preference and Adherence, that explores gaps in awareness and knowledge of…

Read MoreNew Study Assesses Awareness of High Breast Density as a Breast Cancer Risk Factor
  • News

BC Patients Neglected as Province Falls Short on Essential Medication Coverage

  • The Pharma Data
  • September 26, 2024

As British Columbians head to the polls on October 19, the Gastrointestinal Society is drawing attention to a critical issue: BC PharmaCare’s refusal to fund over 30 essential medications that…

Read MoreBC Patients Neglected as Province Falls Short on Essential Medication Coverage
  • Press Releases

Nashville Expansion Announced by Harrow

  • The Pharma Data
  • September 26, 2024

Tennessee Governor Bill Lee, along with Economic and Community Development Commissioner Stuart C. McWhorter and Harrow, Inc. CEO Mark L. Baum, announced today that Harrow is expanding its corporate headquarters…

Read MoreNashville Expansion Announced by Harrow
  • Regulatory

Fujirebio Files FDA Submission for Alzheimer’s Plasma Diagnostic Test

  • The Pharma Data
  • September 26, 2024

Fujirebio has announced that its subsidiary, Fujirebio Diagnostics, Inc., has submitted the Lumipulse® G pTau 217/β-Amyloid 1-42 Plasma Ratio in-vitro diagnostic (IVD) test to the U.S. Food and Drug Administration…

Read MoreFujirebio Files FDA Submission for Alzheimer’s Plasma Diagnostic Test
  • News

Omnicell Names Nnamdi Njoku as Executive Vice President and Chief Operating Officer

  • The Pharma Data
  • September 26, 2024

Omnicell, Inc. (Nasdaq: OMCL), a leader in transforming pharmacy care delivery, has announced the appointment of Nnamdi Njoku as Executive Vice President and Chief Operating Officer, effective October 7, 2024.…

Read MoreOmnicell Names Nnamdi Njoku as Executive Vice President and Chief Operating Officer
  • Press Releases

Medidata Strengthens Focus on Patient Experience with Launch of Patient Payments

  • The Pharma Data
  • September 26, 2024

Medidata, a Dassault Systèmes brand and a leader in clinical trial solutions for the life sciences industry, has introduced Medidata Patient Payments, a new solution designed to simplify the process…

Read MoreMedidata Strengthens Focus on Patient Experience with Launch of Patient Payments
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