An Open Label, Dose Escalation Study to Evaluate the Safety and Efficacy of Localized Injection of STP705 in Adult Patients With Basal Cell Carcinoma

SRN-705-006

This phase 2, open label, dose escalation study is designed to evaluate the safety, tolerability and efficacy of various doses of STP705 administered as localized injection in patients with Basal Cell Carcinoma (BCC). Goals: * To determine the safe and effective recommended dose of STP705 for the treatment of basal cell carcinoma. * Analysis of biomarkers common to BCC formation pathway including TGF-β1 and COX-2.

2020-12-28

2023-02-09

2023-02-09

Completed

Early phase I

32

Inclusion Criteria: Subjects are required to meet all of the following criteria for enrollment into the study: 1. Male or female adult ≥ 18 years of age. 2. Primary, histologically confirmed trunk or extremity (non-peri-orbital/-anogenital/-facial/-scalp) basal cell carcinoma lesion suitable for excision with a minimum diameter of 0.5 cm and with a maximum diameter of 2.0 cm. 3. Histological diagnosis made no more than 6 months prior to the screening visit. 4. Histological biopsy removed ≤25% of the original volume of the target lesion. 5. No other dermatological disease in the BCC target site or surrounding area, which in the opinion of the investigator, could interfere with the study. 6. Willing to refrain from using non-approved lotions or creams on the target site and surrounding area during the treatment period. 7. Willing to refrain from exposure to excessive direct sunlight or ultraviolet light and to avoid the use of tanning parlors for the duration of the study. 8. Laboratory values for the tests (listed in the Study Schedule) within the reference ranges as defined by the central laboratory, or "out of range" test results that is clinically acceptable to the investigator. Ability to follow study instructions and likely to complete all study requirements. 9. Written informed consent obtained, including consent for tissue to be examined and stored by the Central Histology Lab. 10. Written consent to allow photographs of the target BCC lesion to be used as part of the study data and documentation. 11. For females of childbearing potential, a negative pregnancy test at screening and using an acceptable form of birth control (oral / implant/ injectable/ transdermal contraceptives, intrauterine device, condom, diaphragm, abstinence, or a monogamous relationship with a partner who has had a vasectomy). Exclusion Criteria: 1. Pregnant or lactating. 2. Presence of known or suspected systemic cancer. 3. Histological evidence of SCC, or any other non-BCC tumor in the biopsy specimen. 4. Histological evidence of infiltrative or other aggressive histological subtype growth patterns in the biopsy specimen. 5. History of recurrence of the target BCC lesion. 6. Evidence of dermatological disease or confounding skin condition with in 2 cm margin of the target BCC lesion, e.g., SCC, actinic keratosis, rosacea, psoriasis, atopic dermatitis, eczema, xeroderma pigmentosa. 7. Concurrent disease or treatment that suppresses the immune system; 8. Patients with baseline QTC \> 480 msec using Frederica's formula. 9. Chronic medical condition that in the judgment of the investigator(s) would interfere with the performance of the study or would place the patient at undue risk. 10. Known sensitivity to any of the ingredients in the study medication. 11. Use of a tanning beds or other excessive or prolonged exposure to ultraviolet light or direct sunlight during the study. 12. Treatment with systemic chemotherapeutic agents within the 6 months prior to the screening visit. 13. Use of systemic retinoids within the 6 months prior to the screening period. 14. Treatment with systemic immunomodulators or immunosuppressants within the 6 months prior to the screening period. 15. Use of topical immunomodulators within 2 cm of the target BCC lesion within the 4 weeks prior to the screening period. 16. Treatment with the following topical agents within 2 cm of the target BCC lesion within the 4 weeks prior to the screening visit: amino-levulinic acid, 5-fluorouracil, corticosteroids, retinoids, diclofenac, ingenol mebutate, or imiquimod. 17. Treatment with liquid nitrogen, surgical excision (excluding diagnostic incisional biopsy) or curettage within 2 cm of the target BCC lesion during the 4 weeks prior to the screening visit. 18. Evidence of current chronic alcohol or drug abuse. 19. Current enrollment in an investigational drug or device study or participation in such a study within 4 weeks of the screening visit. 20. In the investigator's opinion, evidence of unwillingness, or inability to follow the restrictions and requirements of the protocol and complete the study. 21. Taking any other investigational product within 1 month of first dose of STP705.

{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'SEQUENTIAL', 'interventionModelDescription': 'Participants in the first cohort will attend the study center once weekly for an injection of STP705 into the BCC lesion. The participants will receive injections of STP705 once a week for 6 weeks. The clinician will evaluate the change in tumor size at each treatment visit. At the End of Treatment visit, the residual tumor, or former tumor location, will be excised for analysis.\n\nIn the absence of dose limiting toxicities (DLT), the subsequent cohorts will receive increasing doses of STP705, following the same schedule of administration as the first cohort.', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 32, 'type': 'ACTUAL'}}

2024-03-18