Recent blog posts
Arcturus Therapeutics and the Cystic Fibrosis Foundation are collaborating on the production of ARCT-032, a possible mRNA treatment for Cystic Fibrosis
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Arcturus Therapeutics and the Cystic Fibrosis Foundation are collaborating on the production of ARCT-032, a possible mRNA treatment for Cystic Fibrosis
3 October 2023
Arcturus Therapeutics and the Cystic Fibrosis Foundation continue partnership to further the development of ARCT-032, an experimental mRNA therapy for Cystic Fibrosis.
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Inozyme Pharma reports promising initial results from ongoing INZ-701 phase 1/2 studies in adults with ENPP1 and ABCC6 (PXE) deficiencies
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Inozyme Pharma reports promising initial results from ongoing INZ-701 phase 1/2 studies in adults with ENPP1 and ABCC6 (PXE) deficiencies
3 October 2023
Inozyme Pharma reports encouraging preliminary results from ongoing INZ-701 phase 1/2 studies in adults with ENPP1 and ABCC6 (PXE) deficiencies.
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Omega Therapeutics Shares Optimistic Initial Clinical Results for OTX-2002 in the Continuing MYCHELANGELO™ I Trial
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Omega Therapeutics Shares Optimistic Initial Clinical Results for OTX-2002 in the Continuing MYCHELANGELO™ I Trial
3 October 2023
Omega Therapeutics, Inc. reported positive early findings from the first two doses of its Phase 1/2 MYCHELANGELO™ I study on OTX-2002. The study focuses on hepatocellular carcinoma patients and others with solid tumors linked to the c-MYC gene.
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Roivant Reports Encouraging Preliminary Results for Phase 1 SAD and 300mg Under-skin IMVT-1402 MAD Trials
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Roivant Reports Encouraging Preliminary Results for Phase 1 SAD and 300mg Under-skin IMVT-1402 MAD Trials
3 October 2023
Immunovant, Inc. recently revealed preliminary results of a Phase 1 clinical trial for IMVT-1402.
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Nippon Kayaku and Celltrion declared the Japanese market's endorsement of Adalimumab Biosimilar Monoclonal Antibody
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Nippon Kayaku and Celltrion declared the Japanese market's endorsement of Adalimumab Biosimilar Monoclonal Antibody
3 October 2023
Nippon Kayaku Co., Ltd. and Celltrion Healthcare Japan K.K. have gained approval to manufacture and sell various Adalimumab BS Subcutaneous Injections and Pens in Japan.
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AcuraStem confirms licensing contract with Takeda to progress PIKFYVE treatment methods
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AcuraStem confirms licensing contract with Takeda to progress PIKFYVE treatment methods
3 October 2023
AcuraStem proclaimed it has signed a licensing deal with Takeda.
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Alvotech reveals Japan’s authorization of AVT04 (ustekinumab), a biosimilar counterpart to Stelara®
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Alvotech reveals Japan’s authorization of AVT04 (ustekinumab), a biosimilar counterpart to Stelara®
3 October 2023
Alvotech revealed that its distribution associate in Japan, Fuji Pharma Co., Ltd., has obtained commercialisation authorization for AVT04 (ustekinumab).
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TransCode Therapeutics reports encouraging results in preclinical glioblastoma trials with its main treatment, TTX-MC138
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TransCode Therapeutics reports encouraging results in preclinical glioblastoma trials with its main treatment, TTX-MC138
3 October 2023
TransCode Therapeutics has reported positive findings with its primary treatment candidate, TTX-MC138, in mouse models with human glioblastoma multiforme tumors.
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NMD Pharma has launched a second-phase clinical trial for NMD670 in the treatment of Spinal Muscular Atrophyc
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NMD Pharma has launched a second-phase clinical trial for NMD670 in the treatment of Spinal Muscular Atrophyc
1 October 2023
NMD Pharma A/S has revealed that the initial patient has received their first dose in a Phase II clinical study of the ClC-1 inhibitor NMD670 in individuals affected by spinal muscular atrophy.
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Sandoz's Tyruko® (natalizumab), a unique biosimilar for multiple sclerosis, has been approved by the European Commission
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Sandoz's Tyruko® (natalizumab), a unique biosimilar for multiple sclerosis, has been approved by the European Commission
1 October 2023
Sandoz gains consent from the European Commission for its unique multiple sclerosis biosimilar, Tyruko® (natalizumab) in Europe.
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Lantern Pharma reports initial patient treated in the Phase 1 trial of LP-184 for Advanced Solid Malignancies
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Lantern Pharma reports initial patient treated in the Phase 1 trial of LP-184 for Advanced Solid Malignancies
1 October 2023
Lantern Pharma Inc. has started Phase 1 clinical trial on its experimental drug, LP-184, for advanced solid tumors. This is part of the company's ongoing clinical drug development.
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Escient Pharmaceuticals is now conducting a trial-based study on EP262, a groundbreaking oral MRGPRX2 blocker for chronic hives
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Escient Pharmaceuticals is now conducting a trial-based study on EP262, a groundbreaking oral MRGPRX2 blocker for chronic hives
1 October 2023
Escient Pharmaceuticals commences trial-based study of EP262, an innovative, orally-taken MRGPRX2 blocker for chronic inducible hives.
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