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
             (<class III), inhaled, nasal, and ophthalmic steroids are allowed.
          4. Has an active autoimmune disease that has required systemic treatment in past 2 years
             (i.e., with use of disease modifying agents, corticosteroids, or immunosuppressive
             drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid
             replacement therapy for adrenal or pituitary insufficiency) is not considered a form
             of systemic treatment.
          5. History of Grade 3 or higher immune mediated AEs that were considered drug related to
             prior immunotherapy (e.g., checkpoint inhibitors, co-stimulatory agents).
          6. Infection with HIV-1 or HIV-2. Active hepatitis B (hepatitis B virus [HBV] surface
             antigen positive), hepatitis C (hepatitis C virus [HCV] antibody positive, confirmed
             by HCV ribonucleic acid). Patients with prior history of HBV are eligible if
             quantitative polymerase chain reaction (PCR) for HBV DNA is negative. Patients with
             HCV with undetectable virus after treatment, and those who have minimal viral load
             (<20 IU/ml) at screening and who are being treated with HCV therapy during the full
             study period are eligible.
          7. Has an active infection requiring systemic therapy
          8. Has significant cardiovascular disease, such as:
               1. QT interval corrected for heart rate using Fridericia's formula > 480 msec at
                  screening
               2. History of myocardial infarction, acute coronary syndrome or coronary
                  angioplasty/stenting/bypass grafting within the last 6 months
               3. Congestive heart failure (CHF) New York Heart Association (NYHA) Class II-IV or
                  history of CHF NYHA class III or IV
          9. Patients exhibiting significant respiratory symptoms, those with suspected or known
             serious or severe respiratory conditions and those requiring supplemental oxygen at
             screening.
         10. Receipt of any type of systemic anticancer therapy (including investigational therapy)
             within 3 weeks before the first dose of study drug or 5 times elimination half-life of
             drug, if known, has passed whatever is shorter.
         11. Is currently participating in or has participated in an interventional clinical trial
             with last dose of the investigational compound or device within 3 weeks of the first
             dose of treatment in this current trial. Patients who are in survival follow up can be
             enrolled if the last dose was 3 weeks earlier.
         12. Radiation within 2 weeks before first dose of study treatment. Patients with
             clinically relevant ongoing complications from prior RT are not eligible.
         13. Major surgery within 2 weeks prior to study drug administration; patients must have
             recovered adequately from toxicity and/ or complications per investigator discretion.
         14. Receipt of any live vaccines within 4 weeks prior to first dose of study drug.
         15. Receipt of non-live COVID-19 vaccine within 7 days prior to DLT evaluation because
             vaccine related toxicities could interfere safety assessment.
         16. Any prior treatment with IL-2 based drug.
         17. Has a known hypersensitivity to the components of the study therapy or its analogs.
         18. Has a history or current evidence of any condition therapy, lab abnormality or other
             circumstance that might expose the patient to risk by participating in the trial,
             confound the results of the trial, or interfere with the patient's participation for
             the full duration of the trial.
         19. Has known psychiatric or substance abuse disorders that would interfere with
             cooperation with the requirements of the trial
         20. For women only: pregnant or breastfeeding