Drugs / GL0034
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GL0034

Developed for
type 2 diabetes mellitus
Investigated by
Sun Pharmaceutical Industries, Inc.

Trials 2

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT07385547 Feb → Sep 2026 overdue type 2 diabetes mellitus Sun Pharmaceutical Industries, Inc. Recruiting No outcome recorded
Phase 21 trial
Phase 2 NCT07282743 Jan 2026 → Apr 2027 expected type 2 diabetes mellitus Sun Pharmaceutical Industries, Inc. Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 5

DateIssuerRelease
2025-11-12 Sun Pharmaceutical Industries, Inc. Results Sun Pharma Presents Two Posters on Utreglutide at ObesityWeek® 2025 sunpharma.com ↗
At Week 14, t he GL0034-treated participants achieved mean percent change of -6.8% in body weight, which sustained beyond initial treatment exposure through Week 17.
2025-11-12 Sun Pharmaceutical Industries, Inc. Results Sun Pharma Presents Data from Phase 1b/2a Study of GL0034 at the American Heart Association 2025 Scientific Sessions sunpharma.com ↗
2024-06-22 Sun Pharmaceutical Industries, Inc. Results Sun Pharma’s GL0034 (Utreglutide) Demonstrates Significant Weight Loss, Gluco-metabolic and Lipid Lowering Efficacy in Individuals with Obesity in Oral Presentation at the American Diabetes Association 84th Scientific Sessions sunpharma.com ↗
2023-06-24 Sun Pharmaceutical Industries, Inc. Results ADA GL0034 Data Release sunpharma.com ↗
2020-06-24 Sun Pharmaceutical Industries, Inc. Results Sun Pharma Announces Pre-Clinical Data on GL0034 sunpharma.com ↗
The NCE demonstrated significant outcomes on various diabetic parameters evaluated, viz. glucose reduction, decrease in HbA1c (an important marker for clinical efficacy), augmented insulin secretion, lowering of glucagon level and a marked and meaningful reduction in triglyceride levels.

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 2 sources stand behind the page.

FieldValueCited text
Known as GL0034 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07385547 ↗
1

NCT07282743 ↗

Route Subcutaneous “weekly subcutaneous administration” NCT07282743 ↗