Recent blog posts
Technoderma's TDM-105795 Stage 2 Trial Shows Positive Hair Regrowth in Pattern Baldness
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Technoderma's TDM-105795 Stage 2 Trial Shows Positive Hair Regrowth in Pattern Baldness
18 February 2024
The Stage 2 trial for Technoderma's drug, TDM-105795, reveals positive outcomes for hair regeneration in individuals with pattern baldness.
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Sangamo Therapeutics Unveils Promising Phase 1/2 Results for Fabry Disease Research
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Sangamo Therapeutics Unveils Promising Phase 1/2 Results for Fabry Disease Research
18 February 2024
Sangamo Therapeutics Reveals New Findings from Phase 1/2 STAAR Research for Fabry Disease Indicating Continuous Efficacy and Unique Safety Data.
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CSL & Arcturus' sa-mRNA Technology May Provide Longer Immunity than Standard COVID Boosters
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CSL & Arcturus' sa-mRNA Technology May Provide Longer Immunity than Standard COVID Boosters
18 February 2024
Findings on CSL and Arcturus' sa-mRNA technology suggest extended immunity compared to standard mRNA COVID booster shots.
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Incyte Secures Sole Worldwide Rights for Development and Sales of the Drug Tafasitamab (Monjuvi®)
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Incyte Secures Sole Worldwide Rights for Development and Sales of the Drug Tafasitamab (Monjuvi®)
18 February 2024
Incyte has declared the establishment of an asset acquisition deal with MorphoSys AG, granting Incyte unique worldwide privileges for the drug tafasitamab.
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MorphoSys to merge with Novartis under a new deal, total purchase price set at €2.7 billion in stock value
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MorphoSys to merge with Novartis under a new deal, total purchase price set at €2.7 billion in stock value
18 February 2024
MorphoSys AG has officially declared that it has formed a strategic alliance through a Business Merger Contract with Novartis data42 AG and the principal entity, Novartis AG.
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Positive Outcome for Henlius Phase 1 HLX14 Trial Confirmed
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Positive Outcome for Henlius Phase 1 HLX14 Trial Confirmed
11 February 2024
Henlius Confirms Phase 1 Pharmacokinetic Equivalence Trial of Denosumab HLX14 Achieves Positive Outcome.
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Pliant Therapeutics Reports Favorable Phase 2a Trial Outcomes for Bexotegrast in Liver Fibrosis Suspected Cases
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Pliant Therapeutics Reports Favorable Phase 2a Trial Outcomes for Bexotegrast in Liver Fibrosis Suspected Cases
11 February 2024
Pliant Therapeutics Reports Positive Phase 2a INTEGRIS-PSC Trial Results for Bexotegrast in Primary Sclerosing Cholangitis with Suspected Liver Fibrosis.
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Acepodia Gets US Approval for Innovative Anti-EGFR Cell Therapy Trial, ACE2016
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Acepodia Gets US Approval for Innovative Anti-EGFR Cell Therapy Trial, ACE2016
11 February 2024
Acepodia Reveals US Regulatory Approval for Pioneering Anti-EGFR Allogeneic Cell Treatment Trial, Designated as ACE2016.
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EMA Accepts Submission for Linvoseltamab as Therapy for Recurrent/Resistant Multiple Myeloma
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EMA Accepts Submission for Linvoseltamab as Therapy for Recurrent/Resistant Multiple Myeloma
11 February 2024
Regeneron Pharmaceuticals, Inc. revealed that the European Medicines Agency is reviewing their Marketing Authorization Application for the therapy, linvoseltamab.
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4DMT's Study Shows Promising Outcomes for Eye Injection 4D-150 in Treating Wet Age-Related Macular Degeneration
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4DMT's Study Shows Promising Outcomes for Eye Injection 4D-150 in Treating Wet Age-Related Macular Degeneration
11 February 2024
4DMT Unveils Encouraging Early Results of the Phase 2 PRISM Study for the Eye Injection 4D-150, Indicating Good Safety and Efficacy in Treating Wet Age-Related Macular Degeneration.
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Inmagene Activates Its Right to Secure Sole Global Licensing for IMG-007 and IMG-004 from HUTCHMED
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Inmagene Activates Its Right to Secure Sole Global Licensing for IMG-007 and IMG-004 from HUTCHMED
11 February 2024
Inmagene Biopharmaceuticals has announced its intention to acquire a solo, global license with royalties for IMG-007, a non-eliminating humanized antibody targeting OX40, and IMG-004, a systemically administered BTK inhibitor with non-covalent, reversible mechanisms.
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EMA Approves Review of Tisotumab Vedotin for Advanced Cervical Cancer Therapy
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EMA Approves Review of Tisotumab Vedotin for Advanced Cervical Cancer Therapy
11 February 2024
European Medicines Agency Approves Review of Tisotumab Vedotin Filing for Relapsed or Spreading Cervical Cancer Therapy.
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