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Clinical Trials in the EU / 2024-519005-35-00
Terminated Phase I/II

A Phase 1/2, Randomized, Double-blind, Placebo-controlled 2-part Study of the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of Single Dose ALN-4324 in Overweight to Obese Adult Healthy Volunteers and Multiple Dose ALN-4324 in Overweight to Obese Patients With Type 2 Diabetes Mellitus (T2DM)

2024-519005-35-00 · tracked via the Priya Life Science EU tracker
Sponsor
Alnylam Pharmaceuticals Inc.
Sponsor type
Pharmaceutical company
Therapeutic area
Hormonal diseases
Decision date
10/02/2026
Enrollment target
35
Sites
Germany, Poland

Condition studied

Type 2 Diabetes Mellitus

Investigational medicinal product(s)

Phosphate buffered saline for SC administration

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Frequency of AEs. Safety will also be evaluated through vital signs, ECGs, and clinical laboratory assessments.

Endpoint detail

Change from baseline in HbA1c at Month 6., Matsuda index, and glucose AUC response to glucose tolerance test. Change from baseline in HOMA-IR, Plasma concentrations of ALN-4324 and potential metabolite(s).

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2024-519005-35-00 on CTIS ↗ ← All trials in the EU