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Biomarker Directed Trial of Temozolomide and Stenoparib in Relapsed SCLC
NCT06681220 · VA Office of Research and Development
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
Randomized phase 2, multicenter, biomarker directed clinical trial with a safety lead-in to assess the efficacy of Stenoparib plus Temozolomide (TMZ) in relapsed Small Cell Lung Cancer patients. Participants will receive either a combination of oral Stenoparib at the highest tolerated dose with oral Temozolomide 40mg daily or standard of care Lurbinectedin for 21-day cycles. The Dose limiting toxicity period will be 1 cycle of 21 days. This study will explore if the biomarkers the investigators test predict sensitivity to the combination of Stenoparib plus TMZ and therefore leads to a better treatment response. There are two potential tests of biomarkers that can predict who would benefit from the oral combination of Stenoparib with Temozolomide (TMZ), but they have not been evaluated. This study will test for this sensitivity using a biomarker (found in the blood that may be related to how a person reacts to a drug). The study will include 9 participants for the safety evaluation of the Stenoparib+TMZ group and 5 participants for the standard of care Lurbinectedin safety group. We will first determine safety dose for the experiment arm which, will include 3 groups with 3 participants in each group. Three doses of Stenoparib will be evaluated for toxicity. The initial starting dose of Stenoparib will be 200mg po QD. Once the maximum tolerated dose has been determined, participants will be assigned to one of the two groups in the phase 2 portion. Group 1 will be patients that test negative for the biomarker and will receive treatment with Lurbinectedin as per standard of care guidelines. Group 2 will be patients that test positive for the biomarker that will be randomly assigned to either the combination of Stenoparib plus Temozolomide (TMZ) or Lurbinectedin.
Eligibility criteria
Inclusion Criteria:
* Age 18 years or older at the time of consent.
* Histological or cytological diagnosis of extensive-stage small cell lung cancer.
* Patients must have received one prior line of systemic therapy.
* Patients must have received first-line therapy with Carboplatin and Etoposide.
* If patient is re-treated with Carboplatin and Etoposide at least 6 months or more after first regimen, this will still be considered one line of
* treatment and they will qualify for this trial.
* Patients could have received immunotherapy in combination with the chemotherapy regimen.
* Patients who have received Tarlatamab as second line treatment are allowed.
* ECOG Performance status 0-2.
* Measurable disease as per RECIST v1.1 (NOTE: Previously irradiated lesions are eligible as a target lesion only if there is documented progression of the lesion after irradiation).
* Adequate bone marrow, liver, and renal function, as assessed by the following laboratory requirements:
* ANC 1.5
* Platelets 100 × 109/L
* Hemoglobin 9 g/dL or 5.6 mmol/L
* Aspartate transaminase and alanine transaminase 2.5 × upper limit of normal (ULN), \<5× in patients with known liver metastases
* Serum total bilirubin 1.5 × ULN, 1.5-3.0 × ULN may be included appropriate starting dose adjustment to 200 mg daily.
* Creatinine \<1.5 × ULN or estimated glomerular filtration rate (GFR) 50 ml/min by Cockcroft-Gault. Depending on scenario, GFR 30-49 can be --permissible.
* Women of child-bearing potential must not be pregnant or breastfeeding and must have a negative pregnancy test within 72 hours of cycle 1 Day 1.
* Male and female subjects of child-bearing potential must agree to use a double-barrier method of birth control from the screening visit through 180 days after the last dose of study drug.
* Male subjects of child-bearing potential must agree to use a double-barrier method of birth control including use a male condom (and should also be advised of the benefit for a female partner to use a highly effective method of contraception as a condom may break or leak) and must agree to refrain from donating sperm from screening visit through at least 90 days after the last dose of study drug.
* Previously treated or asymptomatic brain metastases are allowed.
Exclusion Criteria:
* Unstable or clinically significant concurrent medical condition, psychiatric illness or social situation that would, in the opinion of the investigator, jeopardize the safety of a subject and/or their compliance with the protocol.
* Clinically significant acute infection requiring systemic antibacterial, antifungal, or antiviral therapy. (Suppressive therapy for chronic infections allowed, for example: Subjects with HIV/AIDS with adequate antiviral therapy to control viral load would be allowed. Subjects with viral hepatitis with controlled viral load would be allowed while on suppressive antiviral therapy.)
* Prior exposure to lurbinectedin, TMZ or stenoparib.
* Pregnant or breastfeeding.
* Clinical significant cardiovascular disease (ie active)
* Subject with known hypersensitivity to Stenoparib components
* Subject with known history of myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML) are excluded.
* Subject with QTc interval 470 for females, or 450 for males per electrocardiogram (EKG) at screening.
Study design
Enrollment target: 166 participants
Allocation: randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2026-02-23
Estimated completion: 2030-12-31
Last updated: 2026-03-11
Interventions
Combination Product: Stenoparib/TemozolomideDrug: LurbinectedinCombination Product: Stenoparib/Temozolomide
Primary outcomes
- • Progression Free Survival (PFS) (Through study completion up to 2 years.)
- • Recommended Phase 2 dose (Through end of cycle 1 (21 days))
Sponsor
VA Office of Research and Development · fed
Contacts & investigators
ContactShadia Jalal, MD · contact · Shadia.Jalal@va.gov · (317) 274-5500
InvestigatorShadia Jalal, MD · principal_investigator, Richard L. Roudebush VA Medical Center, Indianapolis, IN
All locations (11)
VA Palo Alto Health Care System, Palo Alto, CARecruiting
Palo Alto, California, United States
Jesse Brown VA Medical Center, Chicago, ILNot Yet Recruiting
Chicago, Illinois, United States
Richard L. Roudebush VA Medical Center, Indianapolis, INRecruiting
Indianapolis, Indiana, United States
Robley Rex VA Medical Center, Louisville, KYNot Yet Recruiting
Louisville, Kentucky, United States
VA Ann Arbor Healthcare System, Ann Arbor, MINot Yet Recruiting
Ann Arbor, Michigan, United States
Minneapolis VA Health Care System, Minneapolis, MNNot Yet Recruiting
Minneapolis, Minnesota, United States
Omaha VA Nebraska-Western Iowa Health Care System, Omaha, NENot Yet Recruiting
Omaha, Nebraska, United States
Salisbury W.G. (Bill) Hefner VA Medical Center, Salisbury, NCRecruiting
Salisbury, North Carolina, United States
Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PARecruiting
Philadelphia, Pennsylvania, United States
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PARecruiting
Pittsburgh, Pennsylvania, United States
Michael E. DeBakey VA Medical Center, Houston, TXRecruiting
Houston, Texas, United States