Recent blog posts
The primary endpoint achieved by FASENRA in the Phase III MANDARA trial for eosinophilic granulomatosis with polyangiitis
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The primary endpoint achieved by FASENRA in the Phase III MANDARA trial for eosinophilic granulomatosis with polyangiitis
17 September 2023
Positive high-level results from AstraZeneca's MANDARA Phase III study revealed that FASENRA(benralizumab)
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MBX Biosciences declares encouraging data from a Phase 1 Multiple Ascending Dose study for MBX 2109
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MBX Biosciences declares encouraging data from a Phase 1 Multiple Ascending Dose study for MBX 2109
17 September 2023
MBX Biosciences, Inc. released favorable outcomes from the Phase 1 trial's multiple ascending dose section for MBX 2109.
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EyePoint Pharmaceuticals releases an encouraging safety update for EYP-1901 under PAVIA and DAVIO 2 Phase 2 Clinical Studies
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EyePoint Pharmaceuticals releases an encouraging safety update for EYP-1901 under PAVIA and DAVIO 2 Phase 2 Clinical Studies
17 September 2023
EyePoint Pharmaceuticals, Inc., a company focused on improving life quality for severe eye condition patients, has revealed promising safety data for its key product candidate EYP-1901.
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Ifinatamab Deruxtecan Continues to Demonstrate Durable Responses in Patients with Advanced Small Cell Lung Cancer in Early Trial
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Ifinatamab Deruxtecan Continues to Demonstrate Durable Responses in Patients with Advanced Small Cell Lung Cancer in Early Trial
15 September 2023
Updated results from a subgroup analysis of a phase 1/2 trial showed that ifinatamab deruxtecan (I-DXd) continues to demonstrate durable responses in patients with heavily pretreated advanced small cell lung cancer.
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Bristol Myers Squibb's trial LPA1 Antagonist reduced lung function decline in Progressive Pulmonary Fibrosis patients in a phase 2 study
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Bristol Myers Squibb's trial LPA1 Antagonist reduced lung function decline in Progressive Pulmonary Fibrosis patients in a phase 2 study
15 September 2023
Bristol Myers Squibb's experimental LPA1 Antagonist showed promising results in reducing the rate of lung function decline in the Progressive Pulmonary Fibrosis group in a phase 2 clinical trial.
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Promising results were noted in Phase 1b of the TROPION-Lung04 trial, combining Datopotamab Deruxtecan and Durvalumab for Non-Small Cell Lung Cancer
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Promising results were noted in Phase 1b of the TROPION-Lung04 trial, combining Datopotamab Deruxtecan and Durvalumab for Non-Small Cell Lung Cancer
15 September 2023
Promising clinical responses were observed in TROPION-Lung04's Phase 1b Trial with a combination of Datopotamab Deruxtecan and Durvalumab with Non-Small Cell Lung Cancer.
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The HERTHENA-Lung01 Phase 2 Trial demonstrated significant, lasting effects of Patritumab Deruxtecan in non-small cell lung cancer patients
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The HERTHENA-Lung01 Phase 2 Trial demonstrated significant, lasting effects of Patritumab Deruxtecan in non-small cell lung cancer patients
15 September 2023
The HERTHENA-Lung01 Phase 2 Trial showed that Patritumab Deruxtecan brought about meaningful and durable effects in Patients with non-small cell lung cancer.
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Samsung Bioepis collaborates with Sandoz to market Ustekinumab Biosimilar Candidate
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Samsung Bioepis collaborates with Sandoz to market Ustekinumab Biosimilar Candidate
14 September 2023
Samsung Bioepis Co., Ltd. disclosed it has struck a commercialization pact with Sandoz regarding SB17, a potential biosimilar to Stelarai(ustekinumab).
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OKYO Pharma Concludes Patient Recruitment for Phase 2 Clinical Trial of OK-101 to Dry Eye Syndrome
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OKYO Pharma Concludes Patient Recruitment for Phase 2 Clinical Trial of OK-101 to Dry Eye Syndrome
14 September 2023
OKYO Pharma Limited has successfully enrolled its patient quota for the Phase 2 clinical trial.
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Carrick Therapeutics Declares the U.S. FDA Approval the IND for CT7439, a First-In-Class Inhibitor of CDK12/13
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Carrick Therapeutics Declares the U.S. FDA Approval the IND for CT7439, a First-In-Class Inhibitor of CDK12/13
14 September 2023
Carrick Therapeutics made an announcement that their IND application for CT7439 has been given the green light by U.S FDA.
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Opus Genetics reports the administration of their gene therapy OPGx-LCA5 to the first participant of their phase 1/2 clinical trial
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Opus Genetics reports the administration of their gene therapy OPGx-LCA5 to the first participant of their phase 1/2 clinical trial
14 September 2023
Opus Genetics has administrated to the first patient in its first-in-human Phase 1/2 clinical trial for OPGx-LCA5.
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Eloxx Pharmaceuticals Shares Program Report on Phase 2 Alport Trial involving ELX-02
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Eloxx Pharmaceuticals Shares Program Report on Phase 2 Alport Trial involving ELX-02
14 September 2023
Eloxx Pharmaceuticals, Inc. provided new information on the development of ELX-02 in the context of handling Alport syndrome caused by nonsense mutations.
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