132 Participants Needed

MOMA-341 for Cancer

Recruiting at 10 trial locations
MC
Overseen ByMOMA Clinical Trials
Age: 18+
Sex: Any
Trial Phase: Phase 1
Sponsor: MOMA Therapeutics
Must be taking: Anti-PD(L)1
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 MOMA-341 for individuals with certain advanced or metastatic solid tumors that have specific genetic changes. Researchers aim to determine the safety and efficacy of MOMA-341, both alone and in combination with other treatments. They seek participants who have tried other cancer treatments without success and have solid tumors with specific genetic markers, such as MSI-H or dMMR, which relate to DNA repair. Individuals with solid tumors meeting these criteria and who have previously tried an anti-PD-(L)1 treatment may be suitable candidates for this trial. As a Phase 1 trial, this research focuses on understanding how the treatment works in people, offering the opportunity to be among the first to receive this new therapy.

Do I need to stop my current medications to join the trial?

The trial information does not specify if you need to stop your current medications. However, it mentions that you must be fully recovered from prior therapies, and hormonal therapy is allowed. It's best to discuss your specific medications with the trial team.

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

Research shows that MOMA-341 is being tested for safety in patients with certain advanced solid tumors. It is administered alone or with other treatments, such as chemotherapy and immunotherapy. In these early studies, MOMA-341 has demonstrated some ability to fight cancer cells.

Since it is still in early testing (Phase 1), the main goal is to assess its safety and tolerability. This involves checking for any side effects and understanding how the body processes the medicine. So far, no clear data on side effects have emerged from these studies. This phase focuses on ensuring it is safe for further testing.

In summary, MOMA-341 is in the early stages of safety testing. The focus remains on ensuring it is safe for patients, whether used alone or with other treatments.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about MOMA-341 for cancer because it offers a fresh approach compared to traditional treatments like chemotherapy and surgery. While most standard treatments attack cancer cells directly, often harming healthy cells in the process, MOMA-341 has a unique mechanism that potentially allows it to target cancer cells more precisely. This means it could minimize damage to healthy cells and reduce side effects. Additionally, MOMA-341's versatility is showcased in its combinations with immunotherapy and irinotecan, providing new avenues for enhancing treatment effectiveness.

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

Research has shown that MOMA-341 may be promising for treating certain cancers with specific genetic features. In this trial, participants may receive MOMA-341 as a monotherapy, which lab studies have found to shrink tumors more effectively at higher doses. Another treatment arm involves MOMA-341 combined with chemotherapy, such as irinotecan, which increases DNA damage in cancer cells, making them more sensitive to treatment. Additionally, some participants will receive MOMA-341 with immunotherapy, potentially enhancing the immune system's ability to attack tumors. Although these findings are preliminary, they suggest that MOMA-341 could be useful for treating some hard-to-treat cancers.12367

Are You a Good Fit for This Trial?

This trial is for adults with advanced or metastatic solid tumors that are MSI-H or dMMR and have worsened after anti-PD-(L)1 therapy. If they can't take anti-PD-(L)1 due to autoimmune conditions, they're still eligible. Participants need at least one measurable tumor, an ECOG performance status of ≤2, recovered from past treatments (except hormonal), proper organ function, and must follow contraception rules.

Inclusion Criteria

I can perform daily activities with little or no assistance.
I have recovered from past cancer treatments, but I may still be on hormonal therapy.
My cancer is advanced, cannot be surgically removed, and has specific genetic changes. I have also not responded to previous immunotherapy.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive MOMA-341 as monotherapy or in combination with irinotecan or immunotherapy in dose-escalation and dose-optimization phases

Up to 35 months
21-day or 28-day cycles

Follow-up

Participants are monitored for safety, tolerability, and clinical activity after treatment

4-8 weeks

Open-label extension (optional)

Participants may opt into continuation of treatment long-term

Long-term

What Are the Treatments Tested in This Trial?

Interventions

  • MOMA-341
Trial Overview The study tests the safety and effects of MOMA-341 taken by mouth alone or with other therapies in patients with specific genetic features in their tumors. It's a Phase 1 trial where dosage is adjusted to find safe levels while monitoring how the body responds to the drug and its impact on cancer.
How Is the Trial Designed?
3Treatment groups
Experimental Treatment
Group I: MOMA-341 in Combination with Irinotecan (Treatment Arm 2)Experimental Treatment2 Interventions
Group II: MOMA-341 in Combination with Immunotherapy (Treatment Arm 3)Experimental Treatment2 Interventions
Group III: MOMA-341 Monotherapy (Treatment Arm 1)Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

MOMA Therapeutics

Lead Sponsor

Trials
1
Recruited
160+

Citations

NCT06974110 | Study of Orally Administered MOMA-341 ...The data from this study conducted in patients with MSI-H or dMMR advanced or metastatic solid tumors, including safety, tolerability, PK/PDx findings, and ...
Phase 1 Study DesignMOMA-341 treatment results in dose-dependent antitumor activity and tumor regression in a SW48 MSI-H colorectal cancer (CRC) xenograft model ( ...
MOMA Therapeutics Announces First Patient Dosed in ...First-in-human study of MOMA-341 focuses on advanced or metastatic solid tumors with high microsatellite instability –.
MOMA Therapeutics Initiates First-in-Human Trial of Werner ...The trial will assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary clinical activity of MOMA-341View drug ...
MOMA Therapeutics doses first patient in trial of cancer drugMOMA-341 is being developed as a treatment for cancers with microsatellite instability such as colorectal, gastric and endometrial cancers. It ...
Study of Orally Administered MOMA-341 in Participants With ...The data from this study conducted in patients with MSI-H or dMMR advanced or metastatic solid tumors, including safety, tolerability, PK/PDx ...
MOMA-341 / MOMA TherapeuticsThe company plans to assess the potential of MOMA-341 as a treatment for patients with cancers demonstrating microsatellite instability (MSI-H).
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security