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Marea Therapeutics to Present Phase 1 Study Results of MAR002 for Acromegaly at ENDO 2026
Marea Therapeutics to Present Phase 1 Study Results of MAR002 for Acromegaly at ENDO 2026
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InduPro Therapeutics Names Amanda J. Redig as Chief Medical Officer to Advance Cancer Therapies
InduPro Therapeutics Names Amanda J. Redig as Chief Medical Officer to Advance Cancer Therapies
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Delphia Therapeutics Appoints David P. Kerstein, M.D., as Chief Medical Officer to Advance Cancer Therapies
Delphia Therapeutics Appoints David P. Kerstein, M.D., as Chief Medical Officer to Advance Cancer Therapies
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Citius Oncology Presents Promising Phase 1 Data on LYMPHIR at ASCO Meeting
Citius Oncology Presents Promising Phase 1 Data on LYMPHIR at ASCO Meeting
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Adcendo and MSD Collaborate on Phase Ib Study for Advanced Solid Tumors
Adcendo and MSD Collaborate on Phase Ib Study for Advanced Solid Tumors
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Kura Oncology's New Cancer Drug Shows Promise, Potential $2 Billion Market Opportunity
Kura Oncology's New Cancer Drug Shows Promise, Potential $2 Billion Market Opportunity
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Alkermes to Present New Data on Psychiatric Treatments at ASCP Annual Meeting
Alkermes to Present New Data on Psychiatric Treatments at ASCP Annual Meeting
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Delphia Therapeutics Appoints David P. Kerstein as Chief Medical Officer to Advance Cancer Therapies
Delphia Therapeutics Appoints David P. Kerstein as Chief Medical Officer to Advance Cancer Therapies
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FDA Approves Brenus Pharma's IND Application for STC-1010 in Metastatic Colorectal Cancer
Brenus Pharma, a biotechnology company specializing in immuno-oncology, has received approval from the U.S. Food and Drug Administration (FDA) for its Investigational New Drug (IND) application for STC-1010. This drug is designed to treat microsatellite stable (MSS) metastatic colorectal cancer (mCRC), a condition affecting approximately 95% of mCRC patients who typically show minimal response to standard immunotherapies. The FDA's approval allows Brenus Pharma to proceed with clinical evaluations in the U.S. under the BreAK-CRC001 study. This development follows European regulatory approvals and initial positive results from early Phase Ia trials. The company plans to present further data at the ESMO annual congress in 2026.
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D Pharmatech Reports Positive Results for Zabopegdutide in MASH Treatment
D Pharmatech Reports Positive Results for Zabopegdutide in MASH Treatment
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Crystalys Therapeutics Initiates Phase 2 Trial for Dotinurad in Gout Patients
Crystalys Therapeutics Initiates Phase 2 Trial for Dotinurad in Gout Patients
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Agios Pharmaceuticals Secures EU Approval for PYRUKYND in Thalassaemia Treatment
Agios Pharmaceuticals Secures EU Approval for PYRUKYND in Thalassaemia Treatment
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