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NCT06233942 · ClinicalTrials.gov registry record · Phase 1

Phase 1a/1b First-in-Human Study of BG-C9074 Alone and in Combination With Other Anticancer Therapies in Patients With Advanced Solid Tumors

A Phase 1 study of Advanced Solid Tumor, sponsored by BeOne Medicines.

Recruiting
Registry status
Phase 1
Development phase
308
Enrollment target
20
Study locations

NCT06233942: Recruiting Phase 1 study of Advanced Solid Tumor, sponsored by BeOne Medicines.

NCT06233942 is a Phase 1 study of Advanced Solid Tumor that is actively recruiting participants, run by BeOne Medicines. The registered enrollment target is 308 participants, above the 191-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (61% higher). The trial reports 20 study locations across 10 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06233942, a Phase 1 study of Advanced Solid Tumor, is actively recruiting participants, sponsored by BeOne Medicines.

RECRUITING
Registry status
Phase 1
Development phase
308 participants
Enrollment target
20
Study locations

Study Summary

This is a first-in-human, dose finding and dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C9074 alone and in combination with other anticancer therapies in patients with advanced solid tumors.

Primary Outcome

Number of participants with AEs and SAEs (as graded by the National Cancer Institute-Common Terminology Criteria for Adverse Events \[NCI-CTCAE\] Version \[v\] 5.0),, including findings from physical examinations, electrocardiograms (ECGs), laboratory assessments, and that meet protocol-defined dose-limiting toxicity criteria.

Conditions Studied

Interventions

  • DRUG Bevacizumab
  • DRUG Tislelizumab
  • DRUG BG-C9074

Study Locations (20)

Other

  • Hospital Sirio Libanes Brasilia - Brasília
  • Liga Norte Riograndene Contra O Cancer - Natal
  • Hospital Sao Lucas Da Pucrs - Porto Alegre
  • Instituto Nacional de Cancer Hospital Do Cancer Ii - Rio de Janerio
  • Fundacao Faculdade Regional de Medicina de Sao Jose Do Rio Preto - São José do Rio Preto
  • Icesp Instituto Do Cancer Do Estado de Sao Paulo Octavio Frias de Oliveira - São Paulo
  • Clinica de Pesquisa E Centro de Estudos Em Oncologia Ginecologica E Mamaria - São Paulo

New South Wales

  • Blacktown Cancer and Haematology Centre - Blacktown
  • Macquarie University - North Ryde
  • Cancer Care Wollongong - Wollongong

Victoria

  • Monash Health - Clayton
  • Cabrini Hospital Malvern - Malvern East
  • Peter Maccallum Cancer Centre - Melbourne

California

  • Usc Norris Comprehensive Cancer Center (Nccc) - Los Angeles

Colorado

  • University of Colorado Cancer Center - Aurora

Florida

  • Florida Cancer Specialist Research Institute Lake Nona - Orlando

Maryland

  • Sidney Kimmel Comprehensive Cancer At Johns Hopkins - Baltimore

Ohio

  • James Cancer Hospital and Solove Research Institute - Columbus

Trial Details

FieldValue
Enrollment Target 308 participants
Start Date 2024-04-12
Est. Completion 2028-05-15
Phase Phase 1
BeOne Medicines

29 total trials

What NCT06233942 shows while recruiting

NCT06233942 is an interventional study that assigns participants to a tested intervention. The registered 308 participants enrollment target is mid-sized for trials with a published cap, above the 191-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (61% higher).

The record links to 1 condition, with Advanced Solid Tumor appearing as the primary indexed condition, and to 3 interventions - of which Bevacizumab is the first listed.

NCT06233942 names 20 study sites across 10 states, led by Other, New South Wales, Victoria.

Frequently Asked Questions

What is clinical trial NCT06233942 about?

NCT06233942 is a clinical study titled "Phase 1a/1b First-in-Human Study of BG-C9074 Alone and in Combination With Other Anticancer Therapies in Patients With Advanced Solid Tumors". This is a first-in-human, dose finding and dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C9074 alone and in combination with other anticancer therapies in patients with advanced solid tumors.

What is the current status of trial NCT06233942?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 308 participants. The study started on 2024-04-12. Estimated completion is 2028-05-15.

What conditions does trial NCT06233942 study?

This clinical trial studies the following conditions: Advanced Solid Tumor.

What interventions are being tested in trial NCT06233942?

The interventions under investigation include: Bevacizumab (DRUG), Tislelizumab (DRUG), BG-C9074 (DRUG).

Who is sponsoring clinical trial NCT06233942?

This trial is sponsored by BeOne Medicines, which has 29 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06233942 being conducted?

This trial has 20 study locations across California, Colorado, Florida, Maryland, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Advanced Solid Tumor

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06233942's enrollment target sits among peer trials

308 36th of 189 higher than 154 of 189 other Advanced Solid Tumor trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Advanced Solid Tumor trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06233942, the US trial registry maintained by the National Library of Medicine. NCT06233942 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.