This study evaluates a fenretinide phospholipid suspension for the treatment of small cell lung cancer (SCLC).
Fenretinide has been shown to be a relatively safe and effective anticancer therapy; however, low fenretinide bioavailability and dose limiting toxicities due to excipients used in previous formulations has impeded its therapeutic utility. The product formulation in the current study (ST-001) is a phospholipid suspension of nanoparticle sized fenretinide. The current study is a Phase 1 trial in in relapsed/refractory small cell lung cancer to determine the clinical activity, safety profile, and pharmacology of ST-001.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
44
Intravenous administration
Intravenous administration
University of Southern California
Los Angeles, California, United States
RECRUITINGHenry Ford Cancer Institute
Detroit, Michigan, United States
RECRUITINGTo evaluate the progression-free survival (PFS) of patients with relapsed or refractory small-cell lung cancer (SCLC) who are treated with ST-001 after receiving at least one prior systemic therapy.
Evaluate progression-free survival (PFS) in patients with relapsed or refractory small-cell lung cancer (SCLC) after prior platinum-based chemotherapy ± immunotherapy who are treated with ST-001 (12.5mg/mL) for IV Infusion, using a Simon 2-stage study design with an interim analysis for futility. PFS is defined as the time from start of treatment to disease progression (increase in tumor size, new metastases) or death.
Time frame: From enrollment to end of treatment is 3 weeks
To describe the toxicity profile of ST-001 in patients with SCLC
Determine the number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time frame: From enrollment to end of treatment is 3 weeks
To observe and record anti-tumor activity of ST-001 in patients with SCLC
Preclinical studies with fenretinide suggest potential efficacy against SCLC. Patients will be carefully monitored for tumor response and symptom relief in addition to safety and tolerability. Objective Response Rate (ORR) and progression-free survival (PFS) will be used as tumor response endpoints in this study.
Time frame: From enrollment to end of treatment is 3 weeks
Objective Response Rate (ORR)
ORR = (Number of patients with complete or partial response) / (Total number of evaluable patients) x 100. Minimum duration of individual patient participation is 3 weeks (one cycle of therapy) to be evaluable for response.
Time frame: From enrollment to end of treatment is 3 weeks
To describe the pharmacokinetics of fenretinide when ST-001 is administered by daily infusion for 5 consecutive days every 3 weeks.
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The endpoint for the pharmacokinetic studies is to assess fenretinide blood plasma levels as a function of administered dose and to determine the following PK parameters: maximum fenretinide concentration (Cmax), time of Cmax (Tmax), volume of distribution (Vd), clearance (CL), elimination and fenretinide half-life (t½).
Time frame: From enrollment to end of treatment is 3 weeks
Cmax
Peak plasma fenretinide concentration (in ng/mL)
Time frame: From enrollment to end of treatment is 3 weeks
Tmax
The time it takes for fenretinide to reach the maximum concentration (Cmax) after drug administration (in hours)
Time frame: From enrollment to end of treatment is 3 weeks
Vd
Volume of distribution; fenretinide's propensity to either remain in the plasma or redistribute to other tissue compartments (in liters)
Time frame: From enrollment to end of treatment is 3 weeks
t½
Fenretinide elimination and half-life; the time it takes for the amount of a drug's active substance in your body to reduce by half (hours)
Time frame: From enrollment to end of treatment is 3 weeks