News about "Ascletis Pharma"

Ascletis Selects Oral ASC30-ASC48 Fixed-Dose Combination for Clinical Development in Obesity

Ascletis Selects Oral ASC30-ASC48 Fixed-Dose Combination for Clinical Development in Obesity

Ascletis Pharma has selected its ASC30-ASC48 fixed-dose combination for clinical development as a once-daily oral therapy for obesity. The dual-target GLP-1R/GIPR candidate demonstrated encouraging preclinical efficacy, with an IND submission to the US FDA planned for Q4 2026.

Ascletis Pharma | 17/07/2026 | By News Bureau 132

Ascletis Submits 2 IND Applications to the US FDA for the Treatment of Obesity

Ascletis Submits 2 IND Applications to the US FDA for the Treatment of Obesity

Ascletis has submitted two IND applications to the US FDA for once-monthly obesity therapies, including ASC36_35, a first-in-class triple-target candidate acting on amylin receptor, GLP-1R and GIPR.

Ascletis Pharma | 06/07/2026 | By Akanki 115

Ascletis Pharma Completes US Phase 2 Enrollment for ASC30 GLP-1R Agonist

Ascletis Pharma Completes US Phase 2 Enrollment for ASC30 GLP-1R Agonist

Ascletis Pharma completes US Phase 2 enrollment for ASC30, an oral GLP-1R agonist for diabetes. The 13-week study evaluates safety, efficacy, and tolerability in 100 patients, with topline results expected in Q3 2026.

Ascletis Pharma | 27/04/2026 | By News Bureau 125

Ascletis Receives FDA IND Clearance for Phase II ASC30 Diabetes Study

Ascletis Receives FDA IND Clearance for Phase II ASC30 Diabetes Study

Ascletis has received US FDA IND clearance to initiate a 13-week phase-II, randomised, double-blind, placebo-controlled, multi-centre study evaluating the efficacy, safety and tolerability of its oral small-molecule GLP-1 candidate ASC30 in participants with diabetes, with enrollment expected to begin in the first quarter of 2026.

Ascletis Pharma | 05/01/2026 | By News Bureau 174


 

 

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