A Study to Examine the Safety of Different Doses of BG-68501 Given to Participants With Advanced-Stage Tumors - Join Clinical Trial NCTNCT06257264
How to Join This Clinical Trial - NCTNCT06257264
Learn how to participate in this PHASE1 trial studying an investigational therapy for Breast Cancer, Small Cell Lung Cancer, Ovarian Cancer, Gastric Cancer, Hormone-receptor-positive Breast Cancer, Hormone Receptor Positive HER-2 Negative Breast Cancer, Advanced Solid Tumor, Endometrial Cancer, Prostate Cancer, TNBC - Triple-Negative Breast Cancer, GastroEsophageal Cancer, Bladder Cancer. This study is currently enrolling participants.
Am I Eligible for This Clinical Trial?
This clinical research study is looking for participants with Breast Cancer, Small Cell Lung Cancer, Ovarian Cancer, Gastric Cancer, Hormone-receptor-positive Breast Cancer, Hormone Receptor Positive HER-2 Negative Breast Cancer, Advanced Solid Tumor, Endometrial Cancer, Prostate Cancer, TNBC - Triple-Negative Breast Cancer, GastroEsophageal Cancer, Bladder Cancer. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.
- Condition Being Studied
- Breast Cancer, Small Cell Lung Cancer, Ovarian Cancer, Gastric Cancer, Hormone-receptor-positive Breast Cancer, Hormone Receptor Positive HER-2 Negative Breast Cancer, Advanced Solid Tumor, Endometrial Cancer, Prostate Cancer, TNBC - Triple-Negative Breast Cancer, GastroEsophageal Cancer, Bladder Cancer
- Treatment Being Tested
- Investigational treatment
- Study Phase
- PHASE1 - Early safety study
- Enrollment Status
- Currently enrolling participants
- Study Identifier
- NCTNCT06257264 - ClinicalTrials.gov Identifier
- Sponsored By
- Study sponsor
What to Expect as a Participant
Participating in this clinical trial involves:
- Initial screening to determine eligibility
- Regular study visits and health assessments
- Receiving the study treatment or placebo
- Medical monitoring and follow-up care
- Contributing to medical research that may help others
- Potential access to new treatments before they're widely available
Clinical Trial Benefits and Compensation
Participants in this clinical research study may receive:
- Close medical monitoring by healthcare professionals
- Access to potential new treatments
- Compensation for time and travel (varies by study)
- No-cost study-related medical care
- The opportunity to help advance medical knowledge
Where Is This Clinical Trial Located?
This study is enrolling participants at 33 locations. Find a study site near you:
Clinical Research Site
Newport Beach, California 92663-4162 - United States
Status: RECRUITING
Clinical Research Site
Lake Mary, Florida 32746-2115 - United States
Status: RECRUITING
Clinical Research Site
Saint Louis, Missouri 63110-1010 - United States
Status: RECRUITING
Clinical Research Site
East Brunswick, New Jersey 08816-4096 - United States
Status: RECRUITING
Clinical Research Site
Sioux Falls, South Dakota 57105-2108 - United States
Status: RECRUITING
Clinical Research Site
Dallas, Texas 75230 - United States
Status: RECRUITING
Clinical Research Site
Blacktown, New South Wales 2148 - Australia
Status: RECRUITING
Clinical Research Site
Darlinghurst, New South Wales 2010 - Australia
Status: RECRUITING
Clinical Research Site
Kingswood, New South Wales 2747 - Australia
Status: RECRUITING
Clinical Research Site
St Leonards, New South Wales 2065 - Australia
Status: RECRUITING
And 23 more locations available. Contact us to find the nearest participating site.
How to Enroll in This Study
To learn more about participating in this PHASE1 clinical trial for Breast Cancer, Small Cell Lung Cancer, Ovarian Cancer, Gastric Cancer, Hormone-receptor-positive Breast Cancer, Hormone Receptor Positive HER-2 Negative Breast Cancer, Advanced Solid Tumor, Endometrial Cancer, Prostate Cancer, TNBC - Triple-Negative Breast Cancer, GastroEsophageal Cancer, Bladder Cancer:
- Review the eligibility criteria with your healthcare provider
- Contact the study team for a pre-screening interview
- Schedule an in-person screening visit if eligible
- Review and sign the informed consent form
- Begin participation in the clinical trial
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