Clinical trials

6

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Clamp Study to Estimate the Relative Potency of GZR33 Versus Insulin Degludec at Steady State

This trial intends to investigate the pharmacodynamics, pharmacokinetics, safety, and tolerability of insulin GZR33 (hereafter referred to as GZR33) and estimate its potency in comparison with insulin degludec.

Participants needed: 12
Trial details
Phase: Phase 1Age: 18-64Biological sex: AllType: InterventionalSponsor: Gan and Lee Pharmaceuticals, USAUpdated: Nov 21, 2025Locations: 2
Eligibility criteria

18-64 years of age [+3]

blood pressure outside the range 90 to 140 mmHg (systolic) or 50 to 99 mmHg (dia... [+4]

Status: Recruiting

Comparison Study of Insulin GZR4 With Insulin Degludec

In this study, the investigational product will be compared with insulin degludec (Tresiba®) and insulin icodec (Awiqli®). The comparator products are approved for the treatment of T2DM in the European Union.

Participants needed: 14
Trial details
Phase: Phase 1Age: 18-70Biological sex: AllType: InterventionalSponsor: Gan and Lee Pharmaceuticals, USAUpdated: Aug 28, 2025Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Efficacy and Safety of GZR18 Every 2 Weeks Versus Tirzepatide and Placebo in Obese or Overweight Participants

This is a Phase 2 study to evaluate the safety and efficacy of 24, 36, and 48 mg GZR18 (Q2W) compared with placebo and 15 mg tirzepatide (QW). The study will evaluate weight management in participants with obesity (BMI ≥30 kg/m2) or who are overweight (BMI ≥27 kg/m2) with weight-related comorbidities (excluding type 2 diabetes mellitus).

Participants needed: 285
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Gan and Lee Pharmaceuticals, USAUpdated: Feb 4, 2025Locations: 20
Eligibility criteria

18 to 75 years of age (both inclusive) at the time of signing the informed conse... [+83]

Status: Not yet recruiting

A Phase I Clinical Study to Evaluate the Effect of GZR18 Injection on the Pharmacokinetics of Oral Metformin Hydrochloride Tablets in Overweight/Obese Subjects

This is a single-center, open-label, fixed-sequence phase I clinical study to evaluate the effect of multiple subcutaneous injections of GZR18 Injection on the pharmacokinetics of multiple oral doses of metformin hydrochloride tablets.

Participants needed: 32
Trial details
Phase: Phase 1Age: 18-50Biological sex: AllType: InterventionalSponsor: Gan and Lee Pharmaceuticals, USAUpdated: Nov 1, 2024
Eligibility criteria

Overweight/obese Chinese subjects, who voluntarily sign the Informed Consent For... [+3]

Subjects with a previous or existing history of heart, liver, kidney, gastrointe... [+7]

Status: Recruiting

A Trial Comparing Efficacy, Tolerability, and Safety of GZR101 Injection Once Daily (OD) and GZR33-70 Injection OD

This trial is conducted in China. The aim of the trial is to compare the efficacy, tolerability, and safety of GZR101 Injection and GZR33-70 Injection in type 2 diabetes inadequately controlled on basal/ premixed insulin once daily at least with or without pre-dinner meal-time insulin.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Gan and Lee Pharmaceuticals, USAUpdated: Aug 19, 2024Locations: 1
Eligibility criteria

1. Signed the informed consent form (ICF) before the trial, fully understanding... [+3]

1.Presence or history of malignant neoplasm prior to screening. [+4]

Status: Recruiting

A Study of GZR4 Injection at Different Injection Sites

This trial is conducted in China. This study is a randomized, single-center, open, three-period crossover trial in healthy subjects to compare the PK, PD, and safety of a single administration of GZR4 at different injection sites (abdomen, deltoid region of upper arm, and thigh).

Participants needed: 24
Trial details
Phase: Phase 1Age: 18-55Biological sex: MaleType: InterventionalSponsor: Gan and Lee Pharmaceuticals, USAUpdated: Aug 12, 2024Locations: 1
Eligibility criteria

1. Signing the informed consent form (ICF) before the trial, fully understanding... [+2]

1. Known or suspected hypersensitivity to investigational medical product(s) or... [+5]