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Compound · clinical trials

Lenbelintide clinical trials

Also listed in trial records as AZD6234
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 6 trials in our USA, China, Canada, Japan, UK, India, Germany, Poland, South Korea, Taiwan, Australia, Brazil, Spain, Sweden, Denmark, Turkey, Israel, France, Italy and Czechia registers that name Lenbelintide as an intervention. Synced 29 Sep 2026
6Current trials
5Recruiting now
1Lead sponsor
20Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Lenbelintide is named as an intervention in 6 current clinical trials in our USA, China, Canada, Japan, UK, India, Germany, Poland, South Korea, Taiwan, Australia, Brazil, Spain, Sweden, Denmark, Turkey, Israel, France, Italy and Czechia registers. 5 are recruiting patients now. The most common phase is Phase 3. The lead sponsor is AstraZeneca. The most-studied condition is Obesity or Overweight. The EU clinical trials register (CTIS) separately lists 1 authorised or ongoing trial.

Trials by status

  • Recruiting583%
  • Active, closed117%

Trials by phase

  • Phase 3350%
  • Phase 1233%
  • Phase 2117%
01

Clinical trials of Lenbelintide

6 trials
StudyPhaseStatusLead sponsorRegisters
A Study to Evaluate Effect of AZD6234 as an Adjunct to Incretin-based Therapies in Adult Participants With Obesity or Overweight With Weight-related Comorbidity With or Without Type 2 Diabetes Mellitus
NCT07776509 · ClinicalTrials.gov ↗ · Obesity or Overweight, Weight-Related Comorbidity, With/Without Diabetes Mellitus, Type 2
Phase 3 Recruiting AstraZeneca UK, USA, China, Sweden, Denmark, Turkey, Canada, Brazil, Japan, Israel
A Study to Evaluate Effect of AZD6234 in Adult Participants With Type 2 Diabetes Mellitus and Obesity or Overweight
NCT07784270 · Obesity or Overweight, Diabetes Mellitus, Type 2
Phase 3 Recruiting AstraZeneca UK, USA, India, China, Germany, Spain, Poland, Canada, Japan, South Korea, Taiwan, Australia
A Study to Evaluate Effect of AZD6234 in Adult Participants With Obesity or Overweight With Weight-related Comorbidity Without Type 2 Diabetes Mellitus
NCT07784725 · ClinicalTrials.gov ↗ · Obesity or Overweight
Phase 3 Recruiting AstraZeneca USA, India, China, Germany, France, Italy, Poland, Czechia, Canada, Brazil, Japan, South Korea, Taiwan, Australia
A Study to Investigate the Effect of AZD6234, AZD9550, and a Combination of AZD9550 and AZD6234 on Pharmacokinetics of Combined Oral Contraceptive Ethinyl Estradiol/Levonorgestrel in Healthy Female Participants Living With Overweight or Obesity
NCT07013643 · ClinicalTrials.gov ↗ · Healthy Participants
Phase 1 Recruiting AstraZeneca USA
A Phase I Study to Investigate the Effect of Hepatic Impairment of AZD9550 and AZD6234
NCT07546760 · ClinicalTrials.gov ↗ · Hepatic Impairment
Phase 1 Recruiting AstraZeneca USA
This is a Multi-centre, Multi-drug, Platform Study in Chinese Participants Living With Obesity / Overweight
NCT07017179 · Obesity/Overweight
Phase 2 Active, closed AstraZeneca China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Lenbelintide in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing Lenbelintide. Many trials are registered in both CTIS and ClinicalTrials.gov, so these are shown separately rather than added to the count above. Trials with a site in Ireland are listed first.

StudyPhaseStatusSponsorCountries
A Phase III Randomised, Double-Blind, Placebo-Controlled Multicentre Trial to Evaluate the Efficacy and Safety of AZD6234 as an Adjunct to Incretin-based Therapies in Participants with Obesity or Overweight with at Least One Weight-Related Comorbidity With or Without Type 2 Diabetes Mellitus
2025-523295-23-00 · Nutritional and Metabolic Diseases
Phase 3 Authorised AstraZeneca AB Sweden, Denmark
03

Conditions studied with Lenbelintide

7 conditions
Obesity or Overweight3Diabetes Mellitus, Type 21Weight-Related Comorbidity1With/Without Diabetes Mellitus, Type 21Hepatic Impairment1Healthy Participants1Obesity/Overweight1
04

Sponsors

lead sponsor per trial
Lead sponsorTrials
AstraZeneca6
05

By country register

RegisterTrialsRecruiting
Clinical trials in USA55
Clinical trials in China43
Clinical trials in Canada33
Clinical trials in Japan33
Clinical trials in UK22
Clinical trials in India22
Clinical trials in Germany22
Clinical trials in Poland22
Clinical trials in South Korea22
Clinical trials in Taiwan22
Clinical trials in Australia22
Clinical trials in Brazil22
Clinical trials in Spain11
Clinical trials in Sweden11
Clinical trials in Denmark11
Clinical trials in Turkey11
Clinical trials in Israel11
Clinical trials in France11
Clinical trials in Italy11
Clinical trials in Czechia11
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers. CTIS does not publish a recruiting flag; its trials may also appear in the registers above.

06

Related compounds

07

Questions about Lenbelintide trials

How many clinical trials are testing Lenbelintide?

6 current trials in our USA, China, Canada, Japan, UK, India, Germany, Poland, South Korea, Taiwan, Australia, Brazil, Spain, Sweden, Denmark, Turkey, Israel, France, Italy and Czechia registers name Lenbelintide (also registered as AZD6234) as a drug or biological intervention, as of the registry sync on 29 September 2026. Completed and withdrawn studies are not counted.

Are Lenbelintide trials recruiting patients?

Yes. 5 of the 6 trials are recruiting: 5 with sites in USA, 3 with sites in China, 3 with sites in Canada, 3 with sites in Japan, 2 with sites in UK, 2 with sites in India, 2 with sites in Germany, 2 with sites in Poland, 2 with sites in South Korea, 2 with sites in Taiwan, 2 with sites in Australia, 2 with sites in Brazil, 1 with sites in Spain, 1 with sites in Sweden, 1 with sites in Denmark, 1 with sites in Turkey, 1 with sites in Israel, 1 with sites in France, 1 with sites in Italy and 1 with sites in Czechia. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Lenbelintide clinical trials?

The lead sponsor is AstraZeneca. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Lenbelintide works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Lenbelintide works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Lenbelintide (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 29 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.