308 Participants Needed

S095035 for Advanced Cancer

Recruiting at 34 trial locations
Id
Overseen ByInstitut de Recherches Internationales Servier (I.R.I.S.), Clinical Studies Department
Age: 18+
Sex: Any
Trial Phase: Phase 1 & 2
Sponsor: Servier Bio-Innovation LLC
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment called S095035, sometimes combined with TNG462, to evaluate its effectiveness against advanced solid tumors. It targets individuals whose tumors have a specific genetic change (a homozygous deletion of MTAP) and who have not responded to standard treatments. The trial includes various cancer types, such as non-small cell lung cancer, biliary tract cancer, pancreatic cancer, and gastroesophageal cancer. Candidates with a confirmed MTAP gene deletion and cancer progression after previous treatments may be suitable participants. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment.

Will I have to stop taking my current medications?

The trial does not specify if you need to stop taking your current medications. However, you must not have received any systemic anticancer treatment or radiotherapy within 2 weeks before starting the trial.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research shows that S095035, whether used alone or with TNG462, is still undergoing safety testing in humans. S095035 blocks an enzyme called MAT2A, linked to tumor growth, while TNG462 targets another enzyme, PRMT5, also involved in tumor cells.

Studies have shown that oral cancer drugs like S095035 have undergone safety checks. Some studies suggest that serious side effects can occur, though they are uncommon. As this is the first human trial for this treatment, researchers are closely monitoring for any side effects.

In this early-stage trial, the main goal is to determine a safe dose by gradually increasing it to observe the body's reaction. While detailed safety data is not yet available, this study is designed to carefully monitor for adverse effects and ensure participant safety.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about S095035 because it introduces a potential game-changer for advanced cancers like Non-Small Cell Lung Cancer, Biliary Tract Cancer, and Pancreatic Ductal Adenocarcinoma. Unlike standard treatments that often involve chemotherapy or radiation, S095035 focuses on unique mechanisms, possibly offering a more targeted approach with fewer side effects. Additionally, the combination of S095035 with TNG462 in some treatment arms suggests a novel strategy to enhance efficacy by attacking cancer cells through multiple pathways. This innovative approach could lead to improved outcomes for patients who have limited options with existing therapies.

What evidence suggests that this trial's treatments could be effective for advanced cancer?

Research has shown that S095035 is designed to block an enzyme called MAT2A. This blockage indirectly stops another enzyme, PRMT5, potentially leading to the death of tumor cells. In this trial, participants with pancreatic ductal adenocarcinoma (PDAC) may receive S095035 as a single-agent treatment, which has shown promise in killing cancer cells. Other participants may receive a combination of S095035 with TNG462, which directly blocks PRMT5. Early findings suggest that this combination could be especially helpful for biliary tract cancer (BTC) and gastroesophageal cancers, showing positive results in studies with cancers missing the MTAP gene. These insights provide hope for treating advanced cancers with limited options.13456

Are You a Good Fit for This Trial?

This trial is for adults with advanced or metastatic solid tumors missing the MTAP gene, who've tried at least one treatment without success and have no other standard options left. They should be in relatively good health (ECOG PS 0-1), expect to live at least three more months, can use effective birth control, and are willing to provide tumor tissue samples.

Inclusion Criteria

Estimated life expectancy ≥3 months
Participants able to comply with highly effective method of birth control requirements
I am fully active or can carry out light work.
See 4 more

Exclusion Criteria

Have a known history of Gilbert's syndrome
I have an active liver or biliary disease.
I have active cancer spread to my brain.
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Dose Escalation

Participants receive escalating doses of S095035 to determine the optimal dose

Duration not specified

Follow-up

Participants are monitored for safety and effectiveness after treatment

Approximately 2 years

What Are the Treatments Tested in This Trial?

Interventions

  • S095035
Trial Overview The study tests S095035, an oral drug designed to inhibit a specific enzyme linked with cancer growth in patients whose tumors lack the MTAP gene. It's an early-stage trial where researchers gradually increase doses to find safe levels.
How Is the Trial Designed?
9Treatment groups
Experimental Treatment
Group I: Phase 2 Arm 2c PDAC - S095035-TNG462 combination dose expansionExperimental Treatment2 Interventions
Group II: Phase 2 Arm 2b Gastroesophageal - S095035-TNG462 combination dose expansionExperimental Treatment2 Interventions
Group III: Phase 2 Arm 2a BTC - S095035-TNG462 combination dose expansionExperimental Treatment2 Interventions
Group IV: Phase 2 Arm 1d Basket arm - S095035 single-agent dose expansionExperimental Treatment1 Intervention
Group V: Phase 2 Arm 1c PDAC - S095035 single-agent dose expansionExperimental Treatment1 Intervention
Group VI: Phase 2 Arm 1b BTC - S095035 single-agent dose expansionExperimental Treatment1 Intervention
Group VII: Phase 2 Arm 1a NSCLC - S095035 single-agent dose expansionExperimental Treatment1 Intervention
Group VIII: Phase 1 Arm 2 - S095035-TNG462 combination dose escalationExperimental Treatment2 Interventions
Group IX: Phase 1 Arm 1 - S095035 single-agent dose escalationExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Servier Bio-Innovation LLC

Lead Sponsor

Trials
9
Recruited
670+

Institut de Recherches Internationales Servier

Collaborator

Trials
91
Recruited
67,100+

Tango Therapeutics, Inc.

Industry Sponsor

Trials
5
Recruited
740+

Published Research Related to This Trial

A study involving 63 cancer outpatients treated with oral anticancer agents revealed that 74.6% reported at least one high-level symptom, highlighting the prevalence of adverse events in this population.
The most commonly reported symptoms included fatigue, psychological disorders, and general pain, indicating that patient-reported outcomes (PROs) are effective for identifying significant side effects and can be integrated into routine oncology care.
Assessment of Patient Reported Outcomes (PROs) in Outpatients Taking Oral Anticancer Drugs Included in the Real-Life Oncoral Program.Collomb, B., Dubromel, A., Caffin, AG., et al.[2022]
In a study of 1,832 patients receiving outpatient oral anticancer drugs, serious adverse effects (SAEs) were reported in 2.8% of cases, with gastrointestinal toxicity being the most common issue.
SAEs typically occurred early in treatment, with a median onset of 32 days, highlighting the need for proactive management of gastrointestinal side effects when administering these chemotherapeutic agents.
Survey of serious adverse events and safety evaluation of oral anticancer drug treatment in Japan: A retrospective study.Kawasumi, K., Kujirai, A., Matsui, R., et al.[2020]
Combining anti-PD-1 or anti-PD-L1 immunotherapy with platinum-based chemotherapy significantly improves outcomes for patients with advanced non-small-cell lung cancer (NSCLC) and small-cell lung cancer (SCLC), based on a systematic review of 9 randomized studies.
While immune-mediated adverse events (AEs) and infusion reactions were more common with the combination therapy, there were no unexpected toxicities, indicating that the treatment is generally safe and manageable with appropriate monitoring.
Toxicity management with combination chemotherapy and programmed death 1/programmed death ligand 1 inhibitor therapy in advanced lung cancer.Hoffner, B., Leighl, NB., Davies, M.[2020]

Citations

UCSF Solid Tumor Trial → S095035 as a Single Agent and ...This is a first-in-human Phase 1/2, multicenter, open-label study of S095035 as single-agent, or in combination with TNG462 in adult participants with ...
S095035 as a Single Agent and in Combination in Adult ...This study aims to test a new study drug, S095035, as a single medication or in combination with another drug called TNG462. Researchers will test these new ...
Chapter 9 - Targeted therapy in biliary tract cancerThis chapter provides a comprehensive overview of targeted therapies in biliary tract cancers (BTC), which encompass cholangiocarcinoma and gallbladder ...
ANZCTR - RegistrationS095035 will be taken orally once daily in 28-day cycles. Treatment: Drugs: TNG462 TNG462 will be taken orally once daily in 28-day cycles.
S095035 for Advanced CancerThis trial is for adults with advanced or metastatic solid tumors missing the MTAP gene, who've tried at least one treatment without success and have no other ...
S095035 as a Single Agent and in Combination in Adult ...This is a first-in-human Phase 1/2, multicenter, open-label study of S095035 as single-agent, or in combination with TNG462 in adult ...
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