Cirtuvivint + Irinotecan for Small Cell Lung Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores whether adding cirtuvivint, a new drug, to the chemotherapy drug irinotecan can help treat small cell lung cancer (SCLC) that has returned after treatment. Researchers aim for this combination to increase cancer cells' sensitivity to treatment, improving response and delaying cancer progression. Individuals treated for SCLC who have experienced a recurrence may be suitable for this study, particularly if their previous treatment ceased to be effective. As a Phase 1 trial, this research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new drug combination.
Do I need to stop my current medications to join the trial?
The trial does not specify if you need to stop all current medications, but you cannot use drugs that strongly affect CYP3A4, like ketoconazole or rifampin, within 10 days before starting the study medication.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research shows that cirtuvivint, when combined with irinotecan, is under study for its safety and effectiveness in treating small cell lung cancer (SCLC). Cirtuvivint targets specific proteins that aid cancer cell growth. Early lab studies showed promise in stopping tumor growth and enhancing cancer cells' responsiveness to chemotherapy.
Currently, clinical trials are testing cirtuvivint to better understand its safety in humans. The early trial stages focus on patient tolerance and identifying possible side effects. Although detailed safety information is still being gathered, this phase suggests careful monitoring of safety before broader testing.
Irinotecan, the other drug in this combination, is already used in cancer treatments and has known side effects, which doctors are experienced in managing. The combination with cirtuvivint is under study to determine if it remains safe and enhances treatment effectiveness. While the complete safety picture is still developing, the trial phase indicates a careful approach to understanding any risks involved.12345Why are researchers excited about this trial's treatments?
Researchers are excited about Cirtuvivint combined with Irinotecan for treating small cell lung cancer because this combination targets the cancer in a unique way. Unlike traditional treatments like chemotherapy, which broadly attacks rapidly dividing cells, Cirtuvivint is a novel agent that specifically disrupts the Wnt signaling pathway, a crucial process that many cancer cells rely on to grow. By combining this with Irinotecan, a well-established chemotherapy drug, the treatment aims to enhance cancer cell death while potentially reducing damage to normal cells. This targeted approach could lead to more effective and less toxic treatment options for patients.
What evidence suggests that this trial's treatments could be effective for small cell lung cancer?
This trial will evaluate the combination of cirtuvivint and irinotecan for treating small cell lung cancer (SCLC) that has returned after initial treatment. Research has shown that this combination targets specific proteins that aid cancer cell growth. Lab studies demonstrated that blocking these proteins halted tumor growth and increased cancer cells' responsiveness to chemotherapy. Although human studies remain limited, early results for this combination are promising in improving treatment response and slowing disease progression. Participants in this trial will receive both cirtuvivint and irinotecan as part of the study treatment.12345
Who Is on the Research Team?
Ramaswamy Govindan, M.D.
Principal Investigator
Washington University School of Medicine
Are You a Good Fit for This Trial?
The SLICK Trial is for individuals with relapsed Small Cell Lung Cancer (SCLC) who have previously undergone treatment. The trial aims to test a new combination of drugs in patients whose cancer has returned after initial therapy.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Phase I Treatment
Cirtuvivint is administered orally on a 5 days on/2 days off schedule at the starting dose level, and on a 2 days/week schedule at other dose levels. Irinotecan is given on Days 1 and 8 of a 21-day cycle.
Phase II Treatment
Cirtuvivint is administered orally per the dose and schedule determined in Phase I. Irinotecan is given on Days 1 and 8 of a 21-day cycle.
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Cirtuvivint
- Irinotecan
Find a Clinic Near You
Who Is Running the Clinical Trial?
Washington University School of Medicine
Lead Sponsor
Biosplice Therapeutics, Inc.
Industry Sponsor