News about Clinical Trials

Common Cholesterol Drug Shows Promise Against Drug-Resistant Breast Cancer

Common Cholesterol Drug Shows Promise Against Drug-Resistant Breast Cancer

Korea University researchers show the cholesterol drug inhibits Mcl-1, suppresses metastasis, and restores chemotherapy sensitivity in preclinical models of aggressive TNBC.

Clinical Trials | 08/01/2026 | By News Bureau 136

Acesion Pharma Begins Phase-II Trial of AP31969 in Atrial Fibrillation

Acesion Pharma Begins Phase-II Trial of AP31969 in Atrial Fibrillation

The Phase-II study of AP31969 by Acesion Pharma will evaluate the efficacy and safety of AP31969, a first-in-class oral SK ion channel inhibitor, in reducing atrial fibrillation burden using continuous cardiac rhythm monitoring.

Clinical Trials | 08/01/2026 | By News Bureau

China Updates Ivonescimab Label After NSCLC Survival Gains

China Updates Ivonescimab Label After NSCLC Survival Gains

China’s drug regulator has approved a label update for Akeso’s ivonescimab, citing Phase III data showing significant improvements in progression-free and overall survival in EGFR-TKI-resistant non-small cell lung cancer patients.<br />

Clinical Trials | 07/01/2026 | By News Bureau 212

HUTCHMED Begins Phase III Trial of Surufatinib-Camrelizumab Combo in Pancreatic Cancer

HUTCHMED Begins Phase III Trial of Surufatinib-Camrelizumab Combo in Pancreatic Cancer

HUTCHMED has initiated the phase-III stage of its phase-II/III clinical trial in China evaluating a combination regimen of surufatinib, camrelizumab, nab-paclitaxel, and gemcitabine as a first-line treatment for patients with metastatic pancreatic ductal adenocarcinoma, with the first patient dosed on 30 December, 2025.

Clinical Trials | 05/01/2026 | By News Bureau

FibroBiologics Files IND Application with US FDA for CYPS317 in Psoriasis

FibroBiologics Files IND Application with US FDA for CYPS317 in Psoriasis

FibroBiologics has filed an Investigational New Drug (IND) application with the US FDA for CYPS317, marking a key step towards initiating clinical development of the therapy for psoriasis, supported by encouraging preclinical data showing reduced disease severity and relapse.

Clinical Trials | 03/01/2026 | By News Bureau

XORTX Unveils New Research on Genome-Wide Pathways in Gout

XORTX Unveils New Research on Genome-Wide Pathways in Gout

XORTX Therapeutics highlighted findings from recent independent, peer-reviewed research showing that multiple genetic factors are linked to over-expression of Xanthine Oxidase (XO), chronically elevated blood uric acid levels, and gout—further reinforcing the company’s strategy of targeting XO to treat gout, kidney, and related diseases.

Clinical Trials | 01/01/2026 | By News Bureau

Senhwa Expands Oncology Manufacturing Focus With CX-5461 - ADC Combination Trial

Senhwa Expands Oncology Manufacturing Focus With CX-5461 - ADC Combination Trial

Senhwa Biosciences, Inc. has announced a significant clinical development milestone with its first-in-class investigational agent Pidnarulex (CX-5461) set to be evaluated in combination with the antibody–drug conjugate trastuzumab deruxtecan (Enhertu) in a phase 1b clinical trial.

Clinical Trials | 30/12/2025 | By Darshana

Diamyd Medical Advances Type I Diabetes Phase III Efficacy Readout by Nine Months

Diamyd Medical Advances Type I Diabetes Phase III Efficacy Readout by Nine Months

Diamyd Medical has aligned with the US FDA to accelerate the primary efficacy readout of its Phase 3 DIAGNODE-III trial in type 1 diabetes from 24 to 15 months, enabling results to be available nine months earlier than previously planned.

Clinical Trials | 30/12/2025 | By News Bureau

KEYTRUDA Plus Padcev Improves Survival Outcomes in MIBC

KEYTRUDA Plus Padcev Improves Survival Outcomes in MIBC

KEYTRUDA plus Padcev significantly improved survival and pathologic complete response rates in cisplatin-eligible patients with muscle-invasive bladder cancer when used before and after surgery.

Clinical Trials | 18/12/2025 | By News Bureau

US FDA Approves Phase III Trial of Cadonilimab Against Nivolumab in Gastric Cancer

US FDA Approves Phase III Trial of Cadonilimab Against Nivolumab in Gastric Cancer

The FDA’s clearance enables a global phase III study evaluating Cadonilimab, in combination with chemotherapy, as a first-line option for HER2-negative, unresectable or metastatic gastric and gastroesophageal junction adenocarcinoma, directly comparing its efficacy to standard chemotherapy with or without Nivolumab.

Clinical Trials | 12/12/2025 | By Akanki 180

 
 

 

 

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