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โ† Trials
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Biomarker Directed Trial of Temozolomide and Stenoparib in Relapsed SCLC

RecruitingPhase 1, Phase 2Ages 18 Years - anyAllVA Office of Research and Development
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In plain words

What the trial is, and whether it could suit you

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

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
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 ร— 109/L * Hemoglobin 9 g/dL or 5.6 mmol/L * Aspartate transaminase and alanine transaminase 2.5 ร— upper limit of normal (ULN), \<5ร— in patients with known liver metastases * Serum total bilirubin 1.5 ร— ULN, 1.5-3.0 ร— ULN may be included appropriate starting dose adjustment to 200 mg daily. * Creatinine \<1.5 ร— 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.
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What it tests

  • Stenoparib/Temozolomide
  • Lurbinectedin
  • Stenoparib/Temozolomide
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Where

11 sites
VA Palo Alto Health Care System, Palo Alto, CA
Palo Alto, United States
Jesse Brown VA Medical Center, Chicago, IL
Chicago, United States
Richard L. Roudebush VA Medical Center, Indianapolis, IN
Indianapolis, United States
Robley Rex VA Medical Center, Louisville, KY
Louisville, United States
VA Ann Arbor Healthcare System, Ann Arbor, MI
Ann Arbor, United States
Minneapolis VA Health Care System, Minneapolis, MN
Minneapolis, United States
Omaha VA Nebraska-Western Iowa Health Care System, Omaha, NE
Omaha, United States
Salisbury W.G. (Bill) Hefner VA Medical Center, Salisbury, NC
Salisbury, United States

โ€ฆand 3 more on ClinicalTrials.gov.

๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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