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The Pharma Data

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The Pharma Data
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BioNTech Reports Promising Phase 2 Results for mRNA Immunotherapy BNT111 in Advanced Melanoma Patients

  • The Pharma Data
  • July 31, 2024

BioNTech Announces Promising Phase 2 Results for mRNA Immunotherapy BNT111 in Advanced Melanoma BioNTech today revealed positive topline data from its ongoing Phase 2 clinical trial (EudraCT No.: 2020-002195-12; NCT04526899)…

Read MoreBioNTech Reports Promising Phase 2 Results for mRNA Immunotherapy BNT111 in Advanced Melanoma Patients
  • Business

WuXi AppTec Reports Stable Operations and Growth in Q2 2024: Revenue Up 16% QoQ, Adjusted Net Profit Up 28.5% QoQ

  • The Pharma Data
  • July 31, 2024

WuXi AppTec Reports First Half 2024 Financial Results WuXi AppTec, a global leader in R&D and manufacturing services for the pharmaceutical and life sciences sectors, has announced its financial results…

Read MoreWuXi AppTec Reports Stable Operations and Growth in Q2 2024: Revenue Up 16% QoQ, Adjusted Net Profit Up 28.5% QoQ
  • Research

New Data: 3 Years of LEQEMBI® Treatment Benefits Early Alzheimer’s Patients

  • The Pharma Data
  • July 31, 2024

Today, Eisai Co. Ltd. presented new findings on lecanemab-irmb (branded as LEQEMBI® in the U.S.) at the Alzheimer’s Association International Conference (AAIC) 2024 in Philadelphia and online. This dual-acting anti-amyloid…

Read MoreNew Data: 3 Years of LEQEMBI® Treatment Benefits Early Alzheimer’s Patients
  • Press Releases

Biogen, Beckman Coulter, and Fujirebio Collaborate on Blood Test for Alzheimer’s Tau Pathology

  • The Pharma Data
  • July 31, 2024

Biogen, Beckman Coulter, and Fujirebio have announced a collaboration to identify and develop blood-based biomarkers for tau pathology in Alzheimer’s disease (AD). The goal is to create new tests that…

Read MoreBiogen, Beckman Coulter, and Fujirebio Collaborate on Blood Test for Alzheimer’s Tau Pathology
  • Press ReleasesRegulatory

Vertex Announces FDA Acceptance of Suzetrigine NDA for Acute Pain

  • The Pharma Data
  • July 31, 2024

Vertex Announces FDA Acceptance of Suzetrigine NDA for Acute Pain Vertex Pharmaceuticals today revealed that the U.S. Food and Drug Administration (FDA) has accepted its New Drug Application (NDA) for…

Read MoreVertex Announces FDA Acceptance of Suzetrigine NDA for Acute Pain
  • News

AMPLIFY Phase III Trial: Fixed-Duration Calquence and Venetoclax, ± Obinutuzumab, Boosts PFS in 1st-Line CLL

  • The Pharma Data
  • July 31, 2024

The interim analysis of the AMPLIFY Phase III trial revealed promising results for AstraZeneca’s Calquence (acalabrutinib) combined with venetoclax, with or without obinutuzumab, in treating chronic lymphocytic leukaemia (CLL). The…

Read MoreAMPLIFY Phase III Trial: Fixed-Duration Calquence and Venetoclax, ± Obinutuzumab, Boosts PFS in 1st-Line CLL
  • Regulatory

FDA Grants Priority Review to Novartis’ Scemblix® for Newly Diagnosed CML

  • The Pharma Data
  • July 31, 2024

Novartis announced that the US Food and Drug Administration (FDA) has granted Priority Review status to Scemblix® (asciminib) for the treatment of newly diagnosed adult patients with Philadelphia chromosome-positive chronic…

Read MoreFDA Grants Priority Review to Novartis’ Scemblix® for Newly Diagnosed CML
  • News

Allergan Aesthetics Celebrates Second Annual JUVÉDERM® Day

  • The Pharma Data
  • July 31, 2024

Allergan Aesthetics is excited to announce the return of JUVÉDERM® Day on Wednesday, August 21. Following the success of its inaugural event, JUVÉDERM® Day offers limited-time deals, savings, and exclusive…

Read MoreAllergan Aesthetics Celebrates Second Annual JUVÉDERM® Day
  • Featured

European Commission Approves Roche’s Vabysmo for Retinal Vein Occlusion (RVO) Treatment

  • The Pharma Data
  • July 31, 2024

The European Commission (EC) has approved Vabysmo® (faricimab) for treating visual impairment caused by macular edema secondary to retinal vein occlusion (RVO), which includes branch RVO and central RVO. This…

Read MoreEuropean Commission Approves Roche’s Vabysmo for Retinal Vein Occlusion (RVO) Treatment
  • Press Releases

Roche Acquires LumiraDx’s Point-of-Care Tech to Boost Primary Care Diagnostics

  • The Pharma Data
  • July 31, 2024

Roche announced today the completion of its acquisition of LumiraDx’s Point-of-Care technology, following the necessary antitrust and regulatory approvals. The acquisition will see Roche integrate LumiraDx’s multi-assay point-of-care platform, along…

Read MoreRoche Acquires LumiraDx’s Point-of-Care Tech to Boost Primary Care Diagnostics
  • Featured

AbbVie Announces Financial Results for Q2 2024

  • The Pharma Data
  • July 29, 2024

AbbVie Reports Strong Second-Quarter 2024 Financial Performance AbbVie has announced its financial results for the second quarter ending June 30, 2024. “Our business continues to excel, with second-quarter outcomes significantly…

Read MoreAbbVie Announces Financial Results for Q2 2024
  • Business

AbbVie Gains EU Approval for SKYRIZI® to Treat Ulcerative Colitis

  • The Pharma Data
  • July 29, 2024

AbbVie Announces European Approval of SKYRIZI® for Ulcerative Colitis AbbVie has received European Commission approval for SKYRIZI® (risankizumab) to treat adults with moderately to severely active ulcerative colitis (UC) who…

Read MoreAbbVie Gains EU Approval for SKYRIZI® to Treat Ulcerative Colitis
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