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A Study to Test the Safety and Tolerability of SBO-154 in Patients With Advanced Solid Tumors.

RECRUITINGPhase 1Sponsored by Sun Pharma Advanced Research Company Limited
Actively Recruiting
PhasePhase 1
SponsorSun Pharma Advanced Research Company Limited
Started2025-08-12
Est. completion2028-08
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations5 sites

Summary

This is a Phase 1 study of SBO-154 in patients with advanced cancers who are unable to tolerate or have not previously responded to standard therapy available in the country. The study involves multiple doses and takes place at several centers.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

1. Willing and able to give written and dated informed consent (or legally acceptable representative/ impartial witness when applicable) and is available for the entire study.
2. Willing and able to comply with the scheduled visits, treatment plan, laboratory testing, study procedures, and restrictions (in the Investigator's opinion), and be accessible for follow-up.
3. Has locally recurrent or metastatic disease (except sarcomas) which has relapsed or progressed following local standard treatment, or for which no standard treatment is available.
4. Has a life expectancy of ≥3 months.

Exclusion Criteria:

1. Any major surgery, as determined by the Investigator, within 4 weeks of SBO-154 administration.
2. Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination.
3. Known or suspected history of significant drug abuse as judged by the Investigator.
4. Has an uncontrolled infection requiring intravenous (IV) antibiotics, antivirals, or antifungals.
5. Known or suspected history of excessive intake of alcohol in the 12 months prior to study entry.
6. Positive exclusion tests: urine pregnancy tests (if applicable), serology tests positive for HIV, HCV, HBsAg (unless they are considered subjects with resolved Hepatitis B and C infection).
7. History of any relevant allergy/ hypersensitivity including known immediate or delayed hypersensitivity reaction or idiosyncrasy to biological agents or drug chemically related to SBO-154 or its excipients.
8. Received an investigational agent within 30 days or 5 half-lives- whichever is shorter prior to SBO-154 administration.

Conditions2

Advanced Solid TumorsCancer

Locations5 sites

Arizona

1 site
Honorhealth Research Institute
Scottsdale, Arizona, 85258
Justin Moser, MD, MBA480-323-1350ssharma@honorhealth.com

California

1 site
Sarcoma Oncology Research Center
Santa Monica, California, 90403
Neil S Chawla, MD310-552-9999schawla@sarcomaoncology.com

Connecticut

1 site
Yale University - Yale Cancer Center
New Haven, Connecticut, 06510
So Y Kim, MD203-407-8002soyeon.kim@yale.edu

Illinois

1 site
Hope And Healing Cancer Services, Llc
Hinsdale, Illinois, 60521
Srilata Gundala, MBBS630-560-0121sgundala@hopenheal.care

Texas

1 site
MD Anderson Cancer Center
Houston, Texas, 77030
Ecaterina Dumbrava, MD713-792-3934eeileana@mdanderson.org

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