BG-75202 for Breast Cancer

SD
Overseen ByStudy Director
Age: 18+
Sex: Any
Trial Phase: Phase 1
Sponsor: BeOne Medicines
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment called BG-75202 for individuals with advanced breast cancer and other solid tumors. Researchers aim to determine if BG-75202, alone or combined with other cancer-fighting drugs, is safe and effective in shrinking tumors. Participants should have advanced breast cancer, must have tried other treatments without success, and should be postmenopausal or receiving ovarian suppression. This trial offers an opportunity for those who have not yet received a CDK4/6 inhibitor and are seeking new options. As a Phase 1 trial, the research focuses on understanding how BG-75202 works in people, offering participants the chance to be among the first to receive this new treatment.

Will I have to stop taking my current medications?

The trial information does not specify if you need to stop taking your current medications. It's best to discuss this with the trial team or your doctor.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research shows that BG-75202 is under study to assess its safety and tolerability. As this treatment remains in the early testing stages, detailed safety information is limited. Early trials primarily aim to determine human safety and establish the correct dosage.

While detailed information from past studies is scarce, the testing of BG-75202 indicates promise in earlier lab or animal research. This trial will evaluate human tolerance and potential side effects.

Participants should note that this marks the first human testing of BG-75202, so researchers will closely monitor for any adverse effects. This careful observation ensures prompt attention to any safety concerns.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about BG-75202 for breast cancer because it offers a novel approach compared to current treatments. Most treatments, like hormone therapies or chemotherapy, target cancer cells directly. However, BG-75202 is being tested in different combinations that uniquely target the pathways and receptors involved in cancer growth. For instance, when combined with a CDK4 inhibitor and an aromatase inhibitor, it aims to disrupt cancer cell division and hormone-driven growth more effectively. Additionally, in combinations with an estrogen receptor antagonist, it could block hormone signals that fuel cancer more comprehensively. This multi-faceted approach has the potential to enhance effectiveness and overcome resistance seen with existing therapies.

What evidence suggests that this trial's treatments could be effective for breast cancer?

Research has shown that BG-75202, a new drug, may help treat breast cancer by targeting proteins that aid cancer growth. Early results suggest this drug can shrink tumors and slow their growth. In this trial, participants will receive BG-75202 in various combinations. Some will receive it with CDK4 and aromatase inhibitors, which studies indicate can enhance treatment effectiveness for certain breast cancer types. For patients with estrogen receptor-positive (ER+) breast cancer, other participants will receive BG-75202 combined with an estrogen receptor antagonist, potentially extending the time they live without cancer worsening. These combinations aim to provide better treatment options for advanced breast cancer.13567

Who Is on the Research Team?

SD

Study Director

Principal Investigator

BeOne Medicines

Are You a Good Fit for This Trial?

This trial is for adults with advanced breast cancer or other solid tumors. Participants must meet specific health criteria to join, but the exact inclusion and exclusion details are not provided here.

Inclusion Criteria

Measurable disease as assessed by Response Evaluation Criteria in Solid Tumors (RECIST) v 1.1
I have advanced cancer and cannot tolerate or have tried all standard treatments.
I have advanced breast cancer and received 1-3 treatments for it, with no more than 2 being chemotherapy.
See 5 more

Exclusion Criteria

I do not have active brain metastasis or leptomeningeal disease.
I have previously been treated with KAT6A/B or KAT7 inhibitors.
I haven't had any cancer other than the one being studied in the last 3 years, or any local cancer recurrence has been treated and is not expected to need treatment during the study.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Dose Escalation and Safety Expansion

Sequential cohorts of increasing dose levels of BG-75202 are evaluated as monotherapy and in combination with other agents

Up to 12 months

Dose Optimization and Expansion

Participants receive BG-75202 in combination with other agents to determine the recommended dose for expansion

Up to 2 years

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • BG-75202
Trial Overview The study is testing BG-75202, a new potential cancer drug, both alone and combined with other treatments like Aromatase Inhibitor, CDK4 Inhibitor, and Estrogen Receptor Antagonist. It aims to assess safety and how well it works against tumors.
How Is the Trial Designed?
5Treatment groups
Experimental Treatment
Group I: Part 2C: Dose Expansion, BG-75202 + CDK4 inhibitor + Aromatase InhibitorExperimental Treatment3 Interventions
Group II: Part 2B: Safety Run-In, BG-75202 + CDK4 inhibitor + Aromatase InhibitorExperimental Treatment3 Interventions
Group III: Part 2A: Dose Optimization, BG-75202 + Estrogen Receptor AntagonistExperimental Treatment2 Interventions
Group IV: Part 1B: Dose Escalation and Safety Expansion, BG-75202 + Estrogen Receptor AntagonistExperimental Treatment2 Interventions
Group V: Part 1A: Dose Escalation and Safety Expansion, BG-75202 MonotherapyExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

BeOne Medicines

Lead Sponsor

Citations

An Investigational Study of BG-75202 Alone and in ...The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor ...
BG-75202 for Breast Cancer · Info for ParticipantsThe purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-75202 ...
BeOne Medicines' New Study on BG-75202: A Potential ...The study aims to assess the safety and preliminary antitumor activity of BG-75202, a KAT6A/B inhibitor, in patients with breast cancer and ...
BeOne joins the Kat6 pack | ApexOncoWhen BeOne's BG-75202 starts phase 1 it will become the fifth KAT6 inhibitor in the clinic, according to OncologyPipeline. Pfizer's prifetrastat ...
KAT6 Inhibitors Market Poised for Significant Growth ...The report provides the total potential number of patients in the indications, such as Breast Cancer, Castrate-resistant Prostate Cancer, Non- ...
An Investigational Study of BG-75202 Alone and in ...The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor ...
BG-75202 - Drug Targets, Indications, PatentsA Phase 1a/1b Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of BG-75202, ...
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security