Recent blog posts
2023 SITC | Junshi Biosciences announced the latest clinical results of PD-1 inhibitor Toripalimab
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2023 SITC | Junshi Biosciences announced the latest clinical results of PD-1 inhibitor Toripalimab
8 November 2023
Recent trial findings of Junshi Biosciences' Toripalimab and Cetuximab combo for treating R/M-HNSCC were shared at the 38th annual SITC meeting in 2023.
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2023 AAO | Innovent Biologics Announces Latest Clinical Data for Dual-Target Ophthalmic New Drugs IBI302 and IBI324
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2023 AAO | Innovent Biologics Announces Latest Clinical Data for Dual-Target Ophthalmic New Drugs IBI302 and IBI324
8 November 2023
Innovent Biologics reported two clinical research outcomes at the 2023 AAO annual meeting on Nov 6, 2023. These include the Phase 2 clinical data for IBI302, an anti-VEGF-anti-complement dual target drug for nAMD treatment, and Phase 1 clinical data for IBI324, an anti-VEGF-A/Ang-2 bispecific antibody for DME treatment.
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The phase 2 clinical trial of Otsuka/Visterra's anti-APRIL monoclonal antibody, sibeprenlimab, for the treatment of IgA nephropathy is published in the NEJM
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The phase 2 clinical trial of Otsuka/Visterra's anti-APRIL monoclonal antibody, sibeprenlimab, for the treatment of IgA nephropathy is published in the NEJM
8 November 2023
Otsuka Pharmaceutical and Visterra recently reported that the full Phase II trial results for sibeprenlimab (VIS649), a treatment for IgA nephropathy, have been published in the NEJM.
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The first participant has been administered HG004 in an international phase 1/2 study against hereditary blindness, as disclosed by Huidagene Therapeutics
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The first participant has been administered HG004 in an international phase 1/2 study against hereditary blindness, as disclosed by Huidagene Therapeutics
8 November 2023
HuidaGene Therapeutics, a global oncology-focused biotech company, has announced its first treatment in its multinational HG004 gene therapy study (STAR study). This phase 1/2a investigation uses CRISPR-influenced programmable genomic drugs to potentially treat inherited retinal dystrophies caused by RPE65 gene mutations.
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The FDA gives the go-ahead to Novartis Cosentyx® - a first biological treatment innovation for hidradenitis suppurativa sufferers in roughly ten years
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The FDA gives the go-ahead to Novartis Cosentyx® - a first biological treatment innovation for hidradenitis suppurativa sufferers in roughly ten years
7 November 2023
Novartis reported FDA's approval of Cosentyx® (secukinumab) for the management of moderate to extreme hidradenitis suppurativa in adult patients.
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The FDA has greenlighted a replicable bioequivalent treatment for various inflammation-related disorders
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The FDA has greenlighted a replicable bioequivalent treatment for various inflammation-related disorders
7 November 2023
The FDA has given its sanction for Wezlana (ustekinumab-auub), considering it a biosimilar and substitute for Stelara (ustekinumab) in treating several inflammatory conditions.
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The FDA has cleared Mersana Therapeutics to resume the Phase 1 clinical trial for XMT-2056, the company announced
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The FDA has cleared Mersana Therapeutics to resume the Phase 1 clinical trial for XMT-2056, the company announced
7 November 2023
The U.S. Food and Drug Administration (FDA) has given permission to resume the Phase 1 clinical trial of XMT-2056, according to Mersana Therapeutics, Inc., a biopharmaceutical firm in the clinical stage.
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Lirum Therapeutics reveals promising preliminary results of targeted clinical treatment LX-101's notable efficacy against children's sarcomas
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Lirum Therapeutics reveals promising preliminary results of targeted clinical treatment LX-101's notable efficacy against children's sarcomas
7 November 2023
Lirum Therapeutics announces encouraging results on LX-101, an innovative, clinical-phase targeted treatment, showing significant preliminary efficacy against children's sarcomas.
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Context Therapeutics has revealed preclinical studies, illustrating the distinct and potent effect of its Claudin 6-focused bispecific antibody CTIM-76
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Context Therapeutics has revealed preclinical studies, illustrating the distinct and potent effect of its Claudin 6-focused bispecific antibody CTIM-76
7 November 2023
Context Therapeutics has revealed promising preclinical results for its research asset, CTIM-76.
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Chimeric Therapeutics reports FDA's approval of IND application for CHM 2101, a new CDH17 CAR T cell treatment targeting advanced GI cancer
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Chimeric Therapeutics reports FDA's approval of IND application for CHM 2101, a new CDH17 CAR T cell treatment targeting advanced GI cancer
7 November 2023
Chimeric Therapeutics has disclosed that the US FDA has given the green light to the IND submission for CHM 2101.
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AceLink has unveiled the initial dosing of a patient in the Phase 2 clinical investigation of AL01211 for the treatment of Fabry Disease
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AceLink has unveiled the initial dosing of a patient in the Phase 2 clinical investigation of AL01211 for the treatment of Fabry Disease
6 November 2023
AceLink Therapeutics announced the initiation of AL01211 dosage for the first patient in its Phase 2 study for Fabry disease in China.
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At the annual SITC meeting, Nimbus Therapeutics unveiled encouraging initial results from a clinical study on an HPK1 inhibitor for solid tumors
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At the annual SITC meeting, Nimbus Therapeutics unveiled encouraging initial results from a clinical study on an HPK1 inhibitor for solid tumors
6 November 2023
Nimbus Therapeutics, LLC has now shared preliminary findings from its ongoing Phase 1/2 trial of NDI-101150, an HPK1 small-molecule inhibitor.
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