Overview
This is a Phase 1/2, open-label, multicenter, dose escalation and expansion study, evaluating the safety, tolerability, pharmacokinetic, preliminary anti-tumor activity, and effects on pharmacodynamic markers following administration of SLC-3010 as monotherapy and in combination with gemcitabine, in patients with various advanced solid tumors.
Eligibility
Inclusion Criteria:
Patients must meet all the following inclusion criteria to be eligible for enrollment into the study:
1. Histologically or cytologically-documented solid tumors that are inoperable locally advanced, metastatic, or recurrent:
* Part 1 Dose Escalation: Patients with any solid tumor who have progressed on or are intolerant to standard therapy, for which no standard therapy is available, or who decline standard therapy.
* Part 2: Dose Expansion: Patients must have received at least one prior line of standard therapy in recurrent/metastatic setting and for whom standard life-prolonging therapies are either not available or are not qualified to receive such therapies. Additional general and tumor specific inclusion and exclusion criteria will apply.
2. Patients who have at least one measurable lesion, as defined by RECIST v1.1.
3. Adult male or female patients ≥18 years of age on day of signing the informed consent form (ICF) or follow local regulatory requirement if the legal age for consenting for study participation is more than 18 years.
4. Patients who are able and willing to provide written informed consent and are willing and able to comply with all study procedures.
5. Patients with life expectancy of ≥3 months.
6. Patients with Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1.
7. Patients who demonstrate adequate organ function as defined.
8. Resolution of any clinically significant toxic effects of prior therapy to Grade 0 or 1 according to the NCI CTCAE v5.0 (exception of alopecia and other AEs that are acceptable in the opinion of the Investigator and after discussion with the Medical Monitor)
9. Willingness of male and female patients of reproductive potential to observe conventional and effective birth control methods with failure rates of \<1% for the duration of treatment and for 3 months (6 months for female patients administering gemcitabine) following the last dose of study treatment. This must include barrier methods such as condom or diaphragm with spermicidal gel. Women of childbearing potential (WOCBP) are defined as following menarche and who are not postmenopausal (and 2 years of nontherapy-induced amenorrhea or surgically sterile). For male patients with a nonpregnant female partner of childbearing potential and a WOCBP, 1 of the following highly effective birth control methods, with a failure rate of less than 1% per year when used consistently and correctly, is recommended:
1. Combined estrogen and progestin containing hormonal contraception associated with inhibition of ovulation given orally, intravaginally, or transdermally
2. Progestin-only hormonal contraception associated with inhibition of ovulation given orally, by injection, or by implant
3. Intrauterine device
4. Intrauterine hormone-releasing system
5. Bilateral tubal occlusion/ligation
6. Vasectomized partner
7. Sexual abstinence Note: Sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study drug. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the study and the preferred and usual lifestyle of the patient.
Birth control methods unacceptable for this study include the following:
1. Periodic abstinence (calendar, symptom-thermal, or post-ovulation methods)
2. Withdrawal (coitus interruptus)
3. Spermicide only
4. Lactational amenorrhea method
5. Sperm donation is prohibited during the duration of participation on this protocol and for 90 days after the last dose of study drug
10. WOCBP must have a documented negative serum or urine pregnancy at screening within 3 calendar days before the first dose of study drug. Females who are not of childbearing potential must have documented:
1. Postmenopausal status, defined as cessation of regular menses for at least 12 months and documented serum follicle stimulating hormone (FSH) levels that are within laboratory reference range for postmenopausal women, or
2. Have undergone a documented hysterectomy or bilateral oophorectomy, or
3. Have medically confirmed ovarian failure.
Exclusion Criteria:
Individuals who meet any of the following exclusion criteria will not be eligible to participate:
1. Prior history of or active malignant disease other than that being treated in this study.
Exceptions: (i) Malignancies that were treated curatively and have not recurred within the past 2 years, or (ii) Completely resected basal cell carcinoma and squamous cell carcinoma of the skin, or (iii) Completely resected carcinoma in situ of any type.
2. Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/ or surgery (including radiosurgery) and stable for at least 4 weeks before first dose of study drug. Note: patients with an incidental finding of an isolated lesion \<1 cm in diameter may be eligible if the lesion does not require treatment per investigator judgment. Eligible patients must be neurologically asymptomatic and without corticosteroids treatment for at least 2 weeks prior to start of first dose of study treatment.
3. Diagnosis of immunodeficiency or receiving chronic systemic steroid therapy, or any immunosuppressive therapy within 7 days prior to first dose of study drug. Topical (\
