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NCT02452385

Phase 1 Study of CM082 in Patients With wAMD: Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy

Suspended Phase 1 Last updated 8 January 2020
What this trial tests

Phase 1 trial testing CM082 tablet in Age-Related Macular Degeneration in 56 participants. Suspended.

Timeline
1 March 2015
Primary endpoint
1 June 2020
1 June 2020

Quick facts

Lead sponsorAnewPharma
PhasePhase 1
StatusSuspended
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment56
Start date1 March 2015
Primary completion1 June 2020
Estimated completion1 June 2020
Sites6 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

AnewPharma — full company profile →

Who can join

50 and older, any sex, with Age-Related Macular Degeneration. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This is a Phase I Dose-Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of CM082 tablets in Chinese Patients With wAMD.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. The Effect of CM082, an Oral Tyrosine Kinase Inhibitor, on Experimental Choroidal Neovascularization in Rats.
    Ren C, Shi H, Jiang J, Liu Q, et al · · 2017 · cited 9× · PMID 29201457 · DOI 10.1155/2017/6145651
  2. Safety and tolerability of oral vorolanib for neovascular (wet) age-related macular degeneration: a phase I, open-label study.
    Gao Y, Lu F, Li X, Dai H, et al · · 2023 · cited 4× · PMID 37041349 · DOI 10.1038/s41433-023-02496-x

Verify or expand the search:

Other recruiting trials for Age-Related Macular Degeneration

Currently open trials in the same condition.

Other AnewPharma trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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