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Zai Lab’s DLL3-Targeting ADC Zoci Earns FDA Orphan Drug Status

  • The Pharma Data
  • August 4, 2026

Zai Lab’s DLL3-Targeting ADC Receives FDA Orphan Drug Designation for Neuroendocrine Carcinomas Zai Lab Limited has announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation…

Read MoreZai Lab’s DLL3-Targeting ADC Zoci Earns FDA Orphan Drug Status
  • Research

Rocket Pharmaceuticals Reports Positive Safety Update for RP-A501 Phase 2 Trial

  • The Pharma Data
  • August 4, 2026

Rocket Pharmaceuticals Reports Positive Early Safety Update for RP-A501 Phase 2 Trial in Danon Disease Rocket Pharmaceuticals, Inc. has announced encouraging early safety results from the first three patients treated…

Read MoreRocket Pharmaceuticals Reports Positive Safety Update for RP-A501 Phase 2 Trial
  • Regulatory

Polpharma Biologics Advances PB016 with FDA and EMA Regulatory Acceptance

  • The Pharma Data
  • August 4, 2026

Polpharma Biologics Advances PB016 as FDA and EMA Accept Biosimilar Applications for Review Polpharma Biologics International AG has announced a significant regulatory milestone with the acceptance of both its Biologics…

Read MorePolpharma Biologics Advances PB016 with FDA and EMA Regulatory Acceptance
  • Regulatory

Bayer Seeks New Indication Approval for Kerendia in China

  • The Pharma Data
  • August 1, 2026

Bayer Submits New Drug Application in China to Expand Finerenone Use for Adults with Non-Diabetic Chronic Kidney Disease Bayer has announced the submission of a New Drug Application (NDA) to…

Read MoreBayer Seeks New Indication Approval for Kerendia in China
  • Research

Novo Nordisk Shares Update on Phase 3 ZEUS Trial

  • The Pharma Data
  • August 1, 2026

Novo Nordisk Reports Topline Results from Phase 3 ZEUS Trial Evaluating Ziltivekimab for Cardiovascular Risk Reduction Novo Nordisk has announced topline findings from its pivotal Phase 3 ZEUS cardiovascular outcomes…

Read MoreNovo Nordisk Shares Update on Phase 3 ZEUS Trial
  • NewsRegulatory

EU Approves Datroway® for First-Line Metastatic TNBC Treatment

  • The Pharma Data
  • August 1, 2026

EU Approval Positions Datroway® as the Only TROP2-Targeted Therapy with Overall Survival Benefit in First-Line Metastatic TNBC The European Commission (EC) has approved Datroway® (datopotamab deruxtecan) as a monotherapy for…

Read MoreEU Approves Datroway® for First-Line Metastatic TNBC Treatment
  • Regulatory

Polpharma Biologics Secures FDA and EMA Review for PB016 Biosimilar

  • The Pharma Data
  • August 1, 2026

Polpharma Biologics’ Vedolizumab Biosimilar PB016 Accepted for FDA and EMA Review, Advancing Access to Biologic Therapy for Inflammatory Bowel Disease Polpharma Biologics International AG has announced that its proposed vedolizumab…

Read MorePolpharma Biologics Secures FDA and EMA Review for PB016 Biosimilar
  • Research

PHC Launches Cell-IQ® CO₂ Incubators with Advanced Humidity Control

  • The Pharma Data
  • August 1, 2026

PHC Corporation of North America Launches Cell-IQ® CO₂ Incubator Series with Advanced Humidity Control and Contamination Prevention PHC Corporation of North America (PHCNA), a leading provider of PHCbi laboratory equipment…

Read MorePHC Launches Cell-IQ® CO₂ Incubators with Advanced Humidity Control
  • News

Contineum Therapeutics Announces Second-Quarter 2026 Financial Results

  • The Pharma Data
  • August 1, 2026

Contineum Therapeutics Reports Second Quarter 2026 Financial Results and Reaffirms Clinical Development Milestones Across Inflammatory and Fibrotic Disease Pipeline Contineum Therapeutics, Inc., a clinical-stage biopharmaceutical company focused on developing differentiated…

Read MoreContineum Therapeutics Announces Second-Quarter 2026 Financial Results
  • Industry Updates

CareDx Announces Q2 2026 Financial Performance

  • The Pharma Data
  • August 1, 2026

CareDx Reports Strong Second Quarter 2026 Results with 52% Revenue Growth and Raises Full-Year Financial Outlook CareDx, Inc. (Nasdaq: CDNA), a leading precision medicine diagnostics company focused on transplant medicine,…

Read MoreCareDx Announces Q2 2026 Financial Performance
  • Regulatory

Meitheal Pharmaceuticals Receives FDA Approval for Garzulys™ Injection

  • The Pharma Data
  • August 1, 2026

Meitheal Pharmaceuticals Secures FDA Approval for Garzulys™ Biosimilar Insulin to Expand Diabetes Care in the U.S. Meitheal Pharmaceuticals, Inc., a Chicago-based biopharmaceutical company focused on the development and commercialization of…

Read MoreMeitheal Pharmaceuticals Receives FDA Approval for Garzulys™ Injection
  • Research

PVP Labs to Showcase Taphalgin® at 2026 Military Health System Research Symposium

  • The Pharma Data
  • August 1, 2026

PVP Labs to Present Taphalgin® Research at 2026 Military Health System Research Symposium, Highlighting a Novel Battlefield Pain Management Approach PVP Labs, a clinical-stage biotechnology company focused on developing innovative…

Read MorePVP Labs to Showcase Taphalgin® at 2026 Military Health System Research Symposium
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  • Pretzel Therapeutics Secures UK Approval to Advance PX578 Into Clinical Trials for POLG-Related Mitochondrial DisordersOctober 31, 2026
  • Enhertu Wins 2026 International Prix Galien Award for Best Biotechnology ProductOctober 31, 2026
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