Recent blog posts
Celltrion USA Launches Cost-Effective Adalimumab Biosimilar as a Budget-Friendly Alternative to HUMIRA®
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Celltrion USA Launches Cost-Effective Adalimumab Biosimilar as a Budget-Friendly Alternative to HUMIRA®
14 May 2024
Celltrion USA now offers a budget-friendly adalimumab-aaty biosimilar as an alternative to HUMIRA® at reduced wholesale prices.
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FDA Grants Approval for WestGene's mRNA Cancer Treatment Vaccine
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FDA Grants Approval for WestGene's mRNA Cancer Treatment Vaccine
14 May 2024
WestGene proudly declares a significant breakthrough as the FDA grants IND approval for its mRNA-based cancer vaccine, WGc-043.
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Revance enters the American medical market by introducing DAXXIFY® to treat cervical dystonia
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Revance enters the American medical market by introducing DAXXIFY® to treat cervical dystonia
14 May 2024
Revance Therapeutics, Inc. has initiated the market release of DAXXIFY (DaxibotulinumtoxinA-lanm) for injection, aimed at treating cervical dystonia.
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Shionogi & Co. and Maze Therapeutics Announce Global Licensing Deal for Innovative Pompe Disease Therapy, MZE001
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Shionogi & Co. and Maze Therapeutics Announce Global Licensing Deal for Innovative Pompe Disease Therapy, MZE001
14 May 2024
Shionogi & Co., Ltd. along with Maze Therapeutics, Inc. have declared a global exclusive licensing deal for MZE001, an innovative therapy aimed at addressing Pompe Disease.
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Kite and Arcellx Propel Forward in Developing Anito-Cel for Multiple Myeloma Treatment Program
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Kite and Arcellx Propel Forward in Developing Anito-Cel for Multiple Myeloma Treatment Program
14 May 2024
Kite has provided numerous important updates regarding their collaborative project on anitocabtagene autoleucel (anito-cel) for treating multiple myeloma.
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CytomX Therapeutics Announces Promising Phase 1a Results for CX-904 in Dose Escalation Study
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CytomX Therapeutics Announces Promising Phase 1a Results for CX-904 in Dose Escalation Study
13 May 2024
CytomX Therapeutics Reports Promising Early Stage 1a Results for its Solo Therapy CX-904 (EGFRxCD3 PROBODY® T-cell Engager) in Dose Escalation Study.
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Freeline Reveals Promising FLT201 Gene Therapy Results for Gaucher Disease at ASGCT's 27th Meeting
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Freeline Reveals Promising FLT201 Gene Therapy Results for Gaucher Disease at ASGCT's 27th Meeting
13 May 2024
Freeline Announces Promising Results from Initial Study of FLT201, New Gene Therapy for Gaucher Disease, at ASGCT's 27th Meeting in a Keynote Speech.
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TScan Therapeutics Begins Phase 1 Trial of TCR-T Therapy in Solid Tumors
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TScan Therapeutics Begins Phase 1 Trial of TCR-T Therapy in Solid Tumors
13 May 2024
TScan Therapeutics has started dosing the first participant in a Phase 1 study to assess TCR-T therapy against solid tumors.
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Fate Therapeutics Begins Phase 1 Trial of FT819 CAR T-cell Therapy in Lupus Patient
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Fate Therapeutics Begins Phase 1 Trial of FT819 CAR T-cell Therapy in Lupus Patient
13 May 2024
Fate Therapeutics Reports Initial Treatment of a Lupus Patient in its Phase 1 Study for the FT819 CAR T-cell Off-the-shelf Therapy.
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Initial Phase 1 Results of ACE1831: First Anti-CD20 Linked Allogeneic Gamma Delta T Cell Therapy for Non-Hodgkin's Lymphoma
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Initial Phase 1 Results of ACE1831: First Anti-CD20 Linked Allogeneic Gamma Delta T Cell Therapy for Non-Hodgkin's Lymphoma
11 May 2024
Acepodia Reveals Initial Results from Phase 1 Study of ACE1831, the First Anti-CD20 Antibody-Linked Allogeneic Gamma Delta T Cell Treatment for Non-Hodgkin’s Lymphoma.
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Aspaveli® (pegcetacoplan) received approval in Europe for new adult PNH patients
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Aspaveli® (pegcetacoplan) received approval in Europe for new adult PNH patients
11 May 2024
Sobi announced that the European Commission has approved Aspaveli® (pegcetacoplan) to treat adults with paroxysmal nocturnal haemoglobinuria and haemolytic anaemia.
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Phanes Therapeutics Partners with Roche for Clinical Trial of PT217 and Anti-PD-L1 Treatment
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Phanes Therapeutics Partners with Roche for Clinical Trial of PT217 and Anti-PD-L1 Treatment
11 May 2024
Phanes Therapeutics, Inc. has entered into a clinical supply deal with Roche to test PT217 alongside an anti-PD-L1 treatment.
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