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Lupin Digital Health Collaborates with Medicover Hospitals to Enhance Post-Discharge Cardiac Care

  • The Pharma Data
  • December 17, 2024

Lupin Digital Health, a wholly owned subsidiary of the global pharmaceutical leader Lupin Limited, has announced a strategic collaboration with Medicover Hospitals to enhance cardiac care for patients in India.…

Read MoreLupin Digital Health Collaborates with Medicover Hospitals to Enhance Post-Discharge Cardiac Care
  • Press Releases

Lupin Acquires 3 Diabetes Trademarks from Boehringer Ingelheim

  • The Pharma Data
  • December 14, 2024

Lupin Limited, a leading global pharmaceutical company, has announced the acquisition of three key anti-diabetes trademarks—GIBTULIO®, GIBTULIO MET®, and AJADUO®—from Boehringer Ingelheim International GmbH. This strategic move is aimed at…

Read MoreLupin Acquires 3 Diabetes Trademarks from Boehringer Ingelheim
  • RegulatoryPress Releases

Neurocrine Announces FDA Approval of CRENESSITY for Congenital Adrenal Hyperplasia

  • The Pharma Data
  • December 14, 2024

Neurocrine Biosciences,has announced that the U.S. Food and Drug Administration (FDA) has approved CRENESSITY™ (crinecerfont) capsules and oral solution for use as an adjunctive treatment to glucocorticoid replacement in adults…

Read MoreNeurocrine Announces FDA Approval of CRENESSITY for Congenital Adrenal Hyperplasia
  • Press Releases

Acoramidis Granted Positive CHMP Opinion for Transthyretin Amyloid Cardiomyopathy Treatment

  • The Pharma Data
  • December 14, 2024

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a positive opinion recommending acoramidis for marketing authorization in the European Union (EU).…

Read MoreAcoramidis Granted Positive CHMP Opinion for Transthyretin Amyloid Cardiomyopathy Treatment
  • News

Takeda Highlights Late-Stage Pipeline Advancing Transformative Treatments Across Multiple Areas

  • The Pharma Data
  • December 14, 2024

Takeda is hosting an investor R&D Day today, starting at 8:30 a.m. JST in Tokyo. The event will highlight the company’s late-stage pipeline, focusing on its transformative potential for patients…

Read MoreTakeda Highlights Late-Stage Pipeline Advancing Transformative Treatments Across Multiple Areas
  • Regulatory

FDA Grants Breakthrough Therapy Designation to Tolebrutinib for Non-Relapsing Secondary Progressive MS

  • The Pharma Data
  • December 14, 2024

The US Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to tolebrutinib for the treatment of adults with non-relapsing secondary progressive multiple sclerosis (nrSPMS). This decision is based…

Read MoreFDA Grants Breakthrough Therapy Designation to Tolebrutinib for Non-Relapsing Secondary Progressive MS
  • Press Releases

Lilly’s Omvoh Receives CHMP Recommendation for Crohn’s Disease Approval

  • The Pharma Data
  • December 14, 2024

Eli Lilly and Company announced that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion recommending Omvoh® (mirikizumab) for approval. Omvoh,…

Read MoreLilly’s Omvoh Receives CHMP Recommendation for Crohn’s Disease Approval
  • Research

AbbVie to Acquire Nimble Therapeutics, Further Strengthening Immunology Pipeline

  • The Pharma Data
  • December 14, 2024

AbbVie has announced a definitive agreement to acquire Nimble Therapeutics, a biotech company specializing in the discovery and development of innovative oral peptide therapies. This acquisition includes Nimble’s lead investigational…

Read MoreAbbVie to Acquire Nimble Therapeutics, Further Strengthening Immunology Pipeline
  • ResearchPress Releases

Merck’s WELIREG Gains EU CHMP Backing for VHL Tumors and Advanced RCC

  • The Pharma Data
  • December 14, 2024

Merck known as MSD outside the United States and Canada, announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion recommending…

Read MoreMerck’s WELIREG Gains EU CHMP Backing for VHL Tumors and Advanced RCC
  • News

Lynparza Shows Survival Benefit in Early Breast Cancer: OlympiA Trial

  • The Pharma Data
  • December 14, 2024

Updated results from the OlympiA Phase III trial revealed that AstraZeneca and MSD’s Lynparza (olaparib) continues to show significant, clinically meaningful improvements in overall survival (OS), invasive disease-free survival (IDFS),…

Read MoreLynparza Shows Survival Benefit in Early Breast Cancer: OlympiA Trial
  • Research

Pfizer’s IBRANCE Extends Progression-Free Survival in HR+, HER2+ Breast Cancer

  • The Pharma Data
  • December 14, 2024

Pfizer and Alliance Foundation Trials, LLC (AFT) recently unveiled findings from the Phase 3 PATINA trial, highlighting the potential of IBRANCE (palbociclib) in improving outcomes for patients with hormone receptor-positive…

Read MorePfizer’s IBRANCE Extends Progression-Free Survival in HR+, HER2+ Breast Cancer
  • Research

Cyrus Biotechnology Announces Redosability of IdeS Protease for IgG-driven Autoimmune Disease

  • The Pharma Data
  • December 12, 2024

Cyrus Biotechnology, Inc. has announced new data demonstrating the potent activity of its engineered IgG-degrading enzyme, CYR241, in a rabbit redosing model. Importantly, the study revealed that CYR241 does not…

Read MoreCyrus Biotechnology Announces Redosability of IdeS Protease for IgG-driven Autoimmune Disease
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