RecruitingPhase 1NCT06710158

Study of SC-102 in Patients With Advanced Solid Tumors

Phase Ⅰ Study to Evaluate the Safety/Tolerability, Pharmacokinetics, and Efficacy of SC-102 in Subjects With Advanced or Metastatic Solid Tumors That Express EphA2

Sponsor

Tianjin ConjuStar Biologics Co., Ltd.

Enrollment

120 participants

Start Date

Dec 5, 2024

Study Type

INTERVENTIONAL

Conditions

Advanced Solid Cancers

Summary

This study will evaluate the safety, PK profile, and anti-cancer efficacy of SC-102 in subjects with advanced solid tumors

Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria10

Subjects voluntarily agree to participate in the study and sign the Informed Consent Form (ICF).
Aged 18 to 75 years at the time of signature of the ICF, without gender limitation.
Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1.
Life expectancy of ≥ 3 months as assessed by the investigator.
Women and men of childbearing potential must be advised and agree to practice effective methods of contraception during the study.
Must be willing and able to comply with the protocol and study procedures.
Acceptable renal, hepatic, hematologic, and coagulation functions.
Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.
Metastatic recurrent histologically confirmed malignant solid tumors and exhausted all appropriate treatment options per local guidelines.
Confirmation of EphA2 expression by the central laboratory prior to enrollment is not required for participants enrolled in the dose escalation study, but required for participants enrolled in the dose expansion study.

Exclusion Criteria15

History of other malignancy(ies) within 3 years before signing the ICF, except for cured basal cell carcinoma or squamous cell carcinoma of the skin, carcinoma in situ of the cervix, papillary carcinoma of the thyroid gland, carcinoma in situ of the duct in situ, or other malignant tumors that have survived without disease for more than 5 years.
Any anticancer treatment, including experimental treatments, within 4 weeks before the first dose of the study drug.
Radiotherapy to >30% of the bone marrow or extensive radiotherapy within 4 weeks, or local radiotherapy (e.g., radiation therapy to the thoracic spine and ribs) within 7 days, prior to the first dose of the study drug.
Uncontrolled central nervous system metastases.
Preexisting treatment-related toxicity Grade ≥ 2 (except Grade 2 alopecia and hypothyroidism stable with hormone replacement therapy).
Preexisting Grade ≥ 2 (as per CTCAE v5.0) sensory or motor neuropathy.
Major surgery within 4 weeks prior to the first dose of the study drug.
History of interstitial lung disease (ILD), preexisting ILD, or the suspected ILD that cannot be ruled out by imaging examination at screening.
Preexisting serious dermatological diseases, or having experienced serious skin toxicities during the prior anti-cancer treatment (e.g., Stevens-Johnson syndrome, toxic Epidermal Necrolysis, etc.).
Active infection requiring systemic therapy within 14 days prior to the first dose of the study drug.
History of thromboembolic events and bleeding disorders ≤ 3 months (e.g., deep vein thrombosis (DVT) or pulmonary embolism (PE)) prior to the first dose of the study drug.
Positive results of virus serology tests.
History of serious cardiovascular and cerebrovascular diseases.
Has received treatment within 2 weeks prior to the first dose of the study drug, or requires ongoing treatment with a medication that is a strong inhibitor or inducer of the cytochrome P450 3A4 (CYP3A4) enzymes.
Known sensitivity to any of the ingredients of the investigational product.