Last reviewed · How we verify

NCT04746612

First in Human Study to Evaluate the Safety, Tolerability of HH30134 in Advanced Solid Tumors

Terminated Phase 1 Last updated 30 March 2023
What this trial tests

Phase 1 trial testing HH30134 in Advanced Solid Tumors in 22 participants. Terminated before completion.

Timeline
8 April 2021
Primary endpoint
24 March 2023
24 March 2023

Quick facts

Lead sponsorHaihe Biopharma Co., Ltd.
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment22
Start date8 April 2021
Primary completion24 March 2023
Estimated completion24 March 2023
Sites4 locations across China, Australia

Drugs / interventions tested

Conditions studied

Sponsor

Haihe Biopharma Co., Ltd. — full company profile →

Who can join

18 and older, any sex, with Advanced Solid Tumors. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and to determine the maximum tolerable dose (MTD) and/or recommended phase 2 dose (RP2D) of HH30134 administered orally on a continuous once daily (QD) schedule in adults patients with advanced solid tumors.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Advanced Solid Tumors

Currently open trials in the same condition.

Other Haihe Biopharma Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04746612.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing