Skip to content
Study details
Enrolling now

A Study to Examine the Safety of Different Doses of BG-68501 Given to Participants With Advanced-Stage Tumors

BeiGene
NCT IDNCT06257264ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

258

Study length

about 4.4 years

Ages

18+

Locations

6 sites in CA, FL, MO +3

About this study

This trial is testing the safety of different doses of a new drug called BG-68501 in people with advanced cancers. The goal is to determine how safe and effective this treatment is, as well as how it works in the body.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take BG-68501
  • 2.Take BGB-43395
  • 3.Take Fulvestrant
PhasePhase 1
DrugFulvestrant
Routeinjection
Primary goalPart 1: Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD) of BG-68501

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low13%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

fulvestrant

Drug routes

injection

Endpoints

Primary: Part 1: Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD) of BG-68501, Part 1: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs), Part 2: Objective Response Rate (ORR)

Secondary: Part 1: Area under the concentration-time curve (AUC) for BG-68501 and BGB-43395, Part 1: Half-life (t1/2) for BG-68501 and BGB-43395, Part 1: Maximum observed plasma concentration (Cmax) for BG-68501 and BGB-43395, Part 1: ORR, Part 2: Number of participants with AEs and SAEs, Parts 1 and 2: Disease Control Rate (DCR), Parts 1 and 2: Duration of Response (DOR)

Body systems

Oncology