Testing BR101 injection in patients with advanced solid tumors
A Phase Ia Open-label, Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Antitumor Activity of BR101 Injection, as a Single Agent in Subjects With Advanced Solid Tumors
This study is testing a new injection called BR101 to see if it can help people with advanced solid tumors who haven't had success with other treatments.
Quick facts
| Phase | Phase 1 |
|---|---|
| Study type | Interventional |
| Enrollment | 36 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | BioRay Pharmaceutical Co., Ltd. Industry-sponsored |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Hangzhou, Zhejiang) |
| Trial ID | NCT06001580 on ClinicalTrials.gov |
What this trial studies
This phase I study evaluates the safety and tolerability of BR101, a monotherapy, in patients with advanced solid tumors. Participants will receive single and multiple doses of BR101 to determine the maximum tolerated dose (MTD) and the recommended phase 2 dose (RP2D). Additionally, the study will explore the pharmacokinetics, immunogenicity, and antitumor activity of BR101. The goal is to assess how well this treatment works in patients who have not responded to standard therapies.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older with advanced or metastatic solid tumors that are not amenable to surgical resection and have failed or been intolerant to standard treatments.
Not a fit: Patients with early-stage tumors that can be surgically removed or those who have not yet undergone standard treatment may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could provide a new therapeutic option for patients with advanced solid tumors who have limited treatment choices.
How similar studies have performed: While this approach is not widely tested, similar studies of novel therapies in advanced solid tumors have shown promise in the past.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients who voluntarily sign the informed consent form with an understanding of the nature, purpose and procedures of the trial, and can comply the protocol; 2. Males and females with an age of or above 18 years; 3. Patients with advanced or metastatic solid tumors diagnosed by pathological histology and / or cytology (cell wax only) who are unable for radical surgical resection, or who have failed to standard treatment or who have been intolerant to standard treatment (disease progression, or intolerant to chemotherapy, targeted therapy, etc.), or who lack effective treatment; 4. At least one measurable lesion according to RECIST V1.1; 5. ECOG score ≤ 1; 6. A recovery of previous treatment releated toxic reactions (except for the residual hair loss effect) to or under Grade 1 (according to CTCAE v 5.0) and a complete recovery of the immune-related adverse effects if the patients received anti-tumor treatment before; 7. Sufficient organ and bone marrow function; 8. The expected survival above 12 weeks; 9. Blood HCG test of females with a reproductive potential should be negative; 10. Fertile men and women must use a highly effective contraceptive methods, and continue the birth control for six months after the last dose. Exclusion Criteria: * . An current active autoimmune disease or history; 2. A history of primary immunodeficiency; 3. An current interstitial lung disease or history (except local interstitial lung disease induced by radiotherapy); 4. An active tuberculosis or history; 5. Any active infection that requires systemic treatment through intravenous infusion within 14 days before first dose; 6. Two or more primary tumors (excluding cured cervical in situ carcinoma, basal cell carcinoma or squamous cell skin cancer, and other tumors that have been treated and stable for more than 5 years); 7. Symptomatic or untreated metastasis in brain or other central nervous system. However, patients with CNS matastasis that has been completed removed and/or be stable or relieved after radiotherapy can be enrolled; 8. Uncontrollable pleural fluid, ascites, or pericardial effusion assesed by the investigator; 9. Patients with any of the following heart diseases: any grade of heart failure assesed by NYHA, severe cardiac arrhythmias requiring treatment, Unstable angina pectoris，myocardial infarction occurred within 3 months before the first dose, QTc≥480 ms, hypertension that cannot in good control, receiving PTCA or CABG within 6 months before the first dose; 10. Patients received anti-tumor therapy or participated in other clinical studies and used other test drugs 28 days before the first dose; Patients received the traditional Chinese medicine within 7 days before the first dose; 11. A history of psychopathy; 12. A history of major surgery or radiotherapy within 28 days before the first dose or expecting to operate a major surgery during the trial, a history of therapeutic radioactive agents within 56 days prior to the first dose; 13. A history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation; 14. Patients who have a bleeding tendency or are receiving thrombolytic or anticoagulant therapy; 15. Patients who had been vaccinated within 28 days before the first dose or intend to be vaccinated during the trial; 16. Patients who had a history of blood donation within 3 months before the first dose, or plan to donate blood during the trial; 17. Patients who need to receive corticosteroids for more than 7 days (methylprednisolone \> 10 mg/d or the equivalent dose) or other immunosuppressants within 14 days before the first dose, except for inhaled corticosteroids; 18. Patients with a positive presence in terms of antibody to human immunodeficiency virus should be excluded; patients with a positive treponema pallidum specific antibody test require a further testing of the treponema pallidum non-specific antibody, and if the result is also positive, the subject shoule be excluded; patients with a positive hepatitis C virus antibody test require a further testing of the hepatitis C virus RNA \[HCV RNA\], and if the result is also positive, the subject shoule be excluded; patients with a positive hepatitis B virus antibody test require a further testing of the hepatitis B virus DNA \[HBV DNA\], and if the result is also positive, the subject shoule be excluded; 19. Patients with diseases affecting intravenous injection and blood sample collection; 20. Pregnant or lactating women; 21. A plan to donate sperm from the signing of ICF to 6 months after the last dose; 22. A situation or a possibility that patients can't comply the protocal; 23. Other situations that are not suitable to attend this trial assesed by the investigator.
Where this trial is running
Hangzhou, Zhejiang
- The Second Affiliated Hospital of Zhejiang University Medical College — Hangzhou, Zhejiang, China (Recruiting)
Study contacts
- Study coordinator: Jian Huang, PhD
- Email: hjys@zju.edu.cn
- Phone: (+86)0571-87783759
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.