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NCT03256331

Evaluate the Safety of BEL-X-HG in Advanced Cancer Patients

Terminated Phase 1 Last updated 1 June 2020
What this trial tests

Phase 1 trial testing BEL-X-HG in Advanced Solid Tumors in 23 participants. Terminated before completion.

Timeline
21 June 2017
Primary endpoint
30 March 2020
30 March 2020

Quick facts

Lead sponsorBelx Bio-Pharmaceutical (Taiwan) Corporation
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Designsequential
Maskingnone
Primary purposetreatment
Enrollment23
Start date21 June 2017
Primary completion30 March 2020
Estimated completion30 March 2020
Sites2 locations across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Belx Bio-Pharmaceutical (Taiwan) Corporation — full company profile →

Who can join

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

Sponsor's own description

This is a Phase I, open-label, uncontrolled, multicenter dose escalation and extension study to determine the maximum tolerated dose (MTD) and dose-limiting toxicity (DLT), to evaluate safety / tolerability and preliminary effects of BEL-X-HG in patients with advanced refractory solid tumors. Dose escalation during the study will be made based on dose-limiting toxicity (DLT).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Advanced Solid Tumors

Currently open trials in the same condition.

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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/NCT03256331.

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