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Empowering the Veterinary Workforce by Broadening Educational Access

  • The Pharma Data
  • October 14, 2024

Veterinary technicians play a vital role in the veterinary field, carrying out important tasks such as assisting in surgeries, conducting diagnostic tests, and providing emergency care. To meet the increasing…

Read MoreEmpowering the Veterinary Workforce by Broadening Educational Access
  • Research

Gilead Shares New Efficacy, Safety, and Demographic Data from PURPOSE 2 Trial at HIV Research for Prevention Conference

  • The Pharma Data
  • October 14, 2024

Gilead Sciences, Inc. (Nasdaq: GILD) has released new data from its pivotal Phase 3 PURPOSE 2 trial (NCT04925752), highlighting the efficacy and safety of lenacapavir, an injectable HIV-1 capsid inhibitor,…

Read MoreGilead Shares New Efficacy, Safety, and Demographic Data from PURPOSE 2 Trial at HIV Research for Prevention Conference
  • News

Gilead to Showcase Antiviral Portfolio and HIV Innovations at IDWeek 2024

  • The Pharma Data
  • October 14, 2024

Gilead Sciences, Inc. has announced the presentation of new findings from its antiviral research and development programs at IDWeek 2024, scheduled for October 16-19. The presentations will include data from…

Read MoreGilead to Showcase Antiviral Portfolio and HIV Innovations at IDWeek 2024
  • Press Releases

Results from Phase 3 TALAPRO-2 Trial Indicate TALZENNA and XTANDI Boost Overall Survival

  • The Pharma Data
  • October 14, 2024

Pfizer Inc. (NYSE: PFE) has announced encouraging topline results from the final prespecified overall survival (OS) analysis of the TALAPRO-2 study, evaluating TALZENNA® (talazoparib), an oral poly ADP-ribose polymerase (PARP)…

Read MoreResults from Phase 3 TALAPRO-2 Trial Indicate TALZENNA and XTANDI Boost Overall Survival
  • Regulatory

FDA Approves Pfizer’s HYMPAVZI for Hemophilia A and B Treatment

  • The Pharma Data
  • October 14, 2024

Pfizer Inc. (NYSE: PFE) has announced that the U.S. Food and Drug Administration (FDA) has approved HYMPAVZI™ (marstacimab-hncq) for routine prophylaxis aimed at preventing or reducing bleeding episodes in adults…

Read MoreFDA Approves Pfizer’s HYMPAVZI for Hemophilia A and B Treatment
  • News

Airsupra Reduces Risk of Severe Asthma Exacerbations in Phase III BATURA Trial

  • The Pharma Data
  • October 14, 2024

AstraZeneca’s Airsupra (albuterol/budesonide) has demonstrated promising outcomes in the BATURA Phase IIIb trial, achieving its primary endpoint by significantly and meaningfully reducing the risk of severe asthma exacerbations when used…

Read MoreAirsupra Reduces Risk of Severe Asthma Exacerbations in Phase III BATURA Trial
  • News

Most Children with SMA Treated with Evrysdi Achieve Motor Milestones, Two-Year Data Shows

  • The Pharma Data
  • October 14, 2024

Roche (SIX: RO, ROG; OTCQX: RHHBY) presented promising two-year findings from the ongoing RAINBOWFISH study at the 29th World Muscle Society (WMS) Congress, held from October 8-12, 2024. The study…

Read MoreMost Children with SMA Treated with Evrysdi Achieve Motor Milestones, Two-Year Data Shows
  • Regulatory

FDA Approves Roche’s Itovebi for Advanced Breast Cancer with PIK3CA Mutation

  • The Pharma Data
  • October 14, 2024

Roche (SIX: RO, ROG; OTCQX: RHHBY) announced that the U.S. Food and Drug Administration (FDA) has approved Itovebi™ (inavolisib) for use in combination with palbociclib (Ibrance®) and fulvestrant to treat…

Read MoreFDA Approves Roche’s Itovebi for Advanced Breast Cancer with PIK3CA Mutation
  • Press Releases

Merck to Present New Data on Vaccines and Infectious Disease at IDWeek 2024

  • The Pharma Data
  • October 14, 2024

Merck (NYSE: MRK), also known as MSD outside the U.S. and Canada, announced plans to present new research at IDWeek 2024 in Los Angeles, CA, from October 16-19. The company…

Read MoreMerck to Present New Data on Vaccines and Infectious Disease at IDWeek 2024
  • News

Merck’s KEYTRUDA Achieves EFS Success in Perioperative Treatment for Head and Neck Cancer

  • The Pharma Data
  • October 14, 2024

Merck (NYSE: MRK), also known as MSD outside the U.S. and Canada, announced today that its Phase 3 KEYNOTE-689 trial met the primary endpoint of event-free survival (EFS) for KEYTRUDA®…

Read MoreMerck’s KEYTRUDA Achieves EFS Success in Perioperative Treatment for Head and Neck Cancer
  • Regulatory

FDA Approves COBENFY How Segal Trials are Transforming Schizophrenia Treatment

  • The Pharma Data
  • October 5, 2024

SSegal Trials is proud to have played a significant role in the FDA approval of COBENFY™ (xanomeline and trospium chloride), a pioneering first-in-class muscarinic agonist developed by Bristol Myers Squibb…

Read MoreFDA Approves COBENFY How Segal Trials are Transforming Schizophrenia Treatment
  • News

AHF Urges Wider Availability of Lenacapavir for Global HIV Treatment

  • The Pharma Data
  • October 5, 2024

The AIDS Healthcare Foundation (AHF) has expressed support for Gilead’s recent decision to expand the availability of lenacapavir, a long-acting HIV treatment, to 120 countries through voluntary licensing agreements with…

Read MoreAHF Urges Wider Availability of Lenacapavir for Global HIV Treatment
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