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The Pharma Data

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The Pharma Data
  • Regulatory

Dupixent (dupilumab) Becomes the First Biologic Treatment Approved in the U.S. for COPD Patients

  • The Pharma Data
  • September 28, 2024

Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) and Sanofi have announced that the U.S. Food and Drug Administration (FDA) has approved Dupixent® (dupilumab) as an add-on maintenance treatment for adults with inadequately…

Read MoreDupixent (dupilumab) Becomes the First Biologic Treatment Approved in the U.S. for COPD Patients
  • Regulatory

FDA Approves Bristol Myers Squibb’s COBENFY for Adult Schizophrenia

  • The Pharma Data
  • September 28, 2024

Bristol Myers Squibb (NYSE: BMY) has received approval from the U.S. Food and Drug Administration (FDA) for COBENFY™ (xanomeline and trospium chloride), marking a significant advancement in the treatment of…

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

FDA Approves Dupixent as the First Biologic Treatment for COPD in the U.S

  • The Pharma Data
  • September 28, 2024

The US Food and Drug Administration (FDA) has approved Dupixent (dupilumab) as an add-on maintenance treatment for adults with chronic obstructive pulmonary disease (COPD) who have an eosinophilic phenotype and…

Read MoreFDA Approves Dupixent as the First Biologic Treatment for COPD in the U.S
  • Regulatory

Tagrisso Receives U.S. Approval for Unresectable Stage III EGFR-Mutated Lung Cancer Patients

  • The Pharma Data
  • September 28, 2024

AstraZeneca’s Tagrisso (osimertinib) has received U.S. approval for the treatment of adult patients with unresectable, Stage III epidermal growth factor receptor-mutated (EGFRm) non-small cell lung cancer (NSCLC), whose disease has…

Read MoreTagrisso Receives U.S. Approval for Unresectable Stage III EGFR-Mutated Lung Cancer Patients
  • Press Releases

Roche’s Gazyva Shows Superior Phase III Results in Lupus Nephritis Treatment

  • The Pharma Data
  • September 28, 2024

Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced positive topline results from the Phase III REGENCY study of Gazyva®/Gazyvaro® (obinutuzumab) in patients with active lupus nephritis. The study revealed that…

Read MoreRoche’s Gazyva Shows Superior Phase III Results in Lupus Nephritis Treatment
  • Press Releases

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
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Latest Posts

  • Incyte Highlights Positive 54-Week Povorcitinib Data at AAD 2026
  • Bristol Myers Squibb Reports Positive Phase 3 SCOUT-HCM Results for Camzyos in Adolescents with Symptomatic oHCM
  • Phase 2 CADENCE Trial Confirms Proof-of-Concept for WINREVAIR™ in CpcPH-HFpEF Patients
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