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The Pharma Data
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Merck
  • Regulatory

Merck Gains Two Positive EU CHMP Opinions for KEYTRUDA

  • The Pharma Data
  • September 20, 2025

Merck Secures Dual Positive CHMP Opinions for KEYTRUDA® in Europe: Subcutaneous Administration and New Head & Neck Cancer Indication Merck (NYSE: MRK), known as MSD outside of the United States…

Read MoreMerck Gains Two Positive EU CHMP Opinions for KEYTRUDA
Bayer
  • Press Releases

Celltrion Launches Omlyclo™ Commercially Across Europe at EADV 2025

  • The Pharma Data
  • September 19, 2025

Celltrion Announces Commercial Availability of Omlyclo™ Across Europe at EADV 2025 Celltrion, Inc. today showcased its longstanding commitment to expanding its biosimilar portfolio in the field of immuno-dermatology by attending…

Read MoreCelltrion Launches Omlyclo™ Commercially Across Europe at EADV 2025
  • News

Layoffs at Six Pharma Companies Could Eliminate Over 39,000 Jobs

  • The Pharma Data
  • September 19, 2025

Layoffs From Just 6 Pharmas Could Wipe Out Over 39,000 Jobs This year, Novo Nordisk and Merck announced significant layoffs, with Novo planning to axe about 9,000 employees and Merck…

Read MoreLayoffs at Six Pharma Companies Could Eliminate Over 39,000 Jobs
  • News

Lexicon Supports Phase III Advancement of Non-Opioid Pain Therapy Following Post-Hoc Analysis

  • The Pharma Data
  • September 19, 2025

Lexicon Backs Phase III Go Decision for Non-Opioid Pain Med With Post-Hoc AnalysisSupporting Lexicon Pharmaceuticals’ decision to advance the non-opioid analgesic pilavapadin into late-stage development—despite a topline miss in March—is…

Read MoreLexicon Supports Phase III Advancement of Non-Opioid Pain Therapy Following Post-Hoc Analysis
  • News

Key Challenges in AAD Sourcing: Ensuring GMP Compliance, Reliable Supply, and Quality Control

  • The Pharma Data
  • September 19, 2025

Key challenges in AAD sourcing: GMP compliance, supply reliability & quality control Amino acid derivatives (AADs) are essential starting materials for solid-phase peptide synthesis, crucial for the development of peptide-based therapeutics…

Read MoreKey Challenges in AAD Sourcing: Ensuring GMP Compliance, Reliable Supply, and Quality Control
  • News

Intellia Completes Phase 3 HAELO Study Enrollment for Lonvo-z in Hereditary Angioedema

  • The Pharma Data
  • September 19, 2025

Intellia Therapeutics Completes Enrollment in the Global Phase 3 HAELO Study of Lonvoguran Ziclumeran (lonvo-z) for Hereditary Angioedema Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing…

Read MoreIntellia Completes Phase 3 HAELO Study Enrollment for Lonvo-z in Hereditary Angioedema
  • Regulatory

EU Approves Biogen’s ZURZUVAE® as First Treatment for Postpartum Depression

  • The Pharma Data
  • September 18, 2025

Biogen Receives European Commission Approval for ZURZUVAE® (zuranolone), the First and Only Treatment Approved for Women with Postpartum Depression in Europe Biogen Inc. (Nasdaq: BIIB) announced that the European Commission (EC)…

Read MoreEU Approves Biogen’s ZURZUVAE® as First Treatment for Postpartum Depression
  • News

Saphnelo Self-Administration TULIP-SC Phase III Trial Hits Primary Endpoint in Lupus Patients

  • The Pharma Data
  • September 18, 2025

Saphnelo self-administration TULIP-SC Phase III trial meets primary endpoint in patients with systemic lupus erythematosus based on an interim analysis Positive high-level results from a pre-specified interim analysis of the…

Read MoreSaphnelo Self-Administration TULIP-SC Phase III Trial Hits Primary Endpoint in Lupus Patients
Roche
  • News

Roche to Acquire 89bio and Its Phase 3 FGF21 Analog for Moderate to Severe MASH

  • The Pharma Data
  • September 18, 2025

Roche enters into a definitive merger agreement to acquire 89bio, and its phase 3 FGF21 analog for the therapy of moderate to severe MASH 89bio’s pegozafermin allows for a potentially…

Read MoreRoche to Acquire 89bio and Its Phase 3 FGF21 Analog for Moderate to Severe MASH
  • Regulatory

EU Approves Deciphera’s ROMVIMZA™ for TGCT Treatment

  • The Pharma Data
  • September 18, 2025

Deciphera Receives European Commission Approval of ROMVIMZA™ (vimseltinib) for the Treatment of Tenosynovial Giant Cell Tumor (TGCT) Ono Pharmaceutical Co., Ltd. (Headquarters: Osaka, Japan; President and COO: Toichi Takino; “Ono”),…

Read MoreEU Approves Deciphera’s ROMVIMZA™ for TGCT Treatment
  • Business

GSK Pledges $30B to Expand U.S. R&D and Manufacturing Capacity

  • The Pharma Data
  • September 18, 2025

GSK Commits $30B To Boost US R&D, Manufacturing Operations The multi-billion, multi-year investment comes as many of GSK’s pharma peers pull away from the U.K., either suspending or completely canceling…

Read MoreGSK Pledges $30B to Expand U.S. R&D and Manufacturing Capacity
  • News

Republicans Intensify Pressure as Monarez Makes Explosive Allegations Against Kennedy

  • The Pharma Data
  • September 18, 2025

Republicans Ratchet Up Pressure as Monarez Levels Damning Allegations Against Kennedy During a hearing in front of the Senate’s HELP committee, Susan Monarez addressed her controversial firing and recalled a…

Read MoreRepublicans Intensify Pressure as Monarez Makes Explosive Allegations Against Kennedy
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