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NCT04228406

Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Efficacy Evaluation of GST-HG161

Status unknown Phase 1 Last updated 14 January 2020
What this trial tests

Phase 1 trial testing GST-HG161 in Solid Tumor in 62 participants. Status unknown.

Timeline
1 July 2019
Primary endpoint
30 September 2020
31 December 2020

Quick facts

Lead sponsorFujian Cosunter Pharmaceutical Co. Ltd
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment62
Start date1 July 2019
Primary completion30 September 2020
Estimated completion31 December 2020
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fujian Cosunter Pharmaceutical Co. Ltd — full company profile →

Who can join

18 and older, any sex, with Solid Tumor or C-Met Mutation-Related Tumors. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Safety, tolerability, pharmacokinetic characteristics, and preliminary efficacy evaluation of the selective c-MET inhibitor GST-HG161 in patients with advanced or metastatic solid tumors: An open, single and multiple administration, dose escalation, and expanded phase I trial

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Solid Tumor

Currently open trials in the same condition.

Other Fujian Cosunter Pharmaceutical Co. Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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