122 Participants Needed

AMXI-5001 for Advanced Cancers

Recruiting at 8 trial locations
BW
Overseen ByBonnie Wettersten, MS
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, AMXI-5001, for people with advanced cancers that haven't responded to other treatments. In the first part, researchers will determine the optimal dose. In the second part, they will assess its safety and effectiveness. This study seeks participants whose cancers have not improved with existing treatments and who are not currently undergoing any cancer treatment. As a Phase 1/Phase 2 trial, participants will be among the first to receive this new treatment, aiding researchers in understanding its effects and measuring its initial effectiveness.

Will I have to stop taking my current medications?

The trial requires that you stop using strong inhibitors or inducers of CYP3A4 (a liver enzyme) within 7 days before starting the study and throughout the trial. This includes some antibiotics, antifungals, anticonvulsants, and grapefruit. Other medications are not specifically mentioned, so it's best to discuss with the trial team.

Is there any evidence suggesting that AMXI-5001 is likely to be safe for humans?

Research shows that AMXI-5001 is being tested for safety in people with advanced cancers. Treatments for these cancers can often cause severe side effects. The trial aims to determine the right dose of AMXI-5001 to minimize these effects.

AMXI-5001 is in the early testing stages, with researchers closely monitoring for any side effects. This phase is crucial to ensure the treatment's safety before larger studies.

Since AMXI-5001 is not yet approved for any condition, its safety profile is not fully known. Participants in the trial will help researchers understand how well people tolerate the treatment and identify potential side effects.12345

Why do researchers think this study treatment might be promising?

AMXI-5001 is unique because it targets cancer cells differently than current treatments. While many existing therapies, like chemotherapy and radiation, work by attacking both healthy and cancerous cells, AMXI-5001 is designed to selectively target cancer cells, potentially reducing side effects. Researchers are excited about its novel mechanism of action, which involves a new active ingredient that may provide more effective results in treating advanced cancers. This targeted approach not only has the potential to improve outcomes but also to enhance the quality of life for patients by minimizing harm to healthy cells.

What evidence suggests that AMXI-5001 might be an effective treatment for advanced cancers?

Research has shown that AMXI-5001 could effectively treat advanced cancers. In studies, AMXI-5001 killed cancer cells in 110 different types of human cancer, including challenging ones like ovarian, prostate, pancreatic, and breast cancer. The treatment attacks and breaks down cancer cells, hindering their survival and growth. Although more research is needed to confirm these benefits in people, early results are promising for those whose cancers have not responded to other treatments. In this trial, all participants will receive AMXI-5001.12367

Who Is on the Research Team?

PM

Pamela Munster, MD

Principal Investigator

AtlasMedx, Incorporated

Are You a Good Fit for This Trial?

This trial is for adults with advanced cancers like ovarian, prostate, pancreatic, or breast cancer that have worsened despite standard treatments. Participants must be over 18 and have a performance status indicating they can care for themselves (ECOG PS 0-1). They should not be on current cancer treatment and must not take certain drugs affecting liver enzymes.

Inclusion Criteria

I am fully active or restricted in physically strenuous activity but can do light work.
My cancer can be measured or evaluated using scans or tests.
My cancer has worsened despite treatment.
See 3 more

Exclusion Criteria

I haven't taken any strong CYP3A4 affecting drugs or eaten grapefruit in the last week.
I do not have any major organ system diseases.
I do not have serious heart disease or abnormal heart tests.
See 2 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 AMXI-5001 to determine the Maximum Tolerated Dose and Recommended Phase 2 Dose

12 months

Dose Expansion

Additional participants receive AMXI-5001 at the recommended dose to further characterize safety and efficacy

12 months

Follow-up

Participants are monitored for safety and effectiveness after treatment

24 months

What Are the Treatments Tested in This Trial?

Interventions

  • AMXI-5001
Trial Overview AMXI-5001 is being tested in two phases: Phase I to find the right dose and Phase II to assess its safety and effectiveness. Patients with advanced malignancies who haven't responded well to other therapies are given escalating doses of AMXI-5001 until an optimal dose is found.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: AMXI-5001 TreatmentExperimental Treatment2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

AtlasMedx, Incorporated

Lead Sponsor

Trials
1
Recruited
120+

Published Research Related to This Trial

Immune-related adverse events (irAEs) are common but mostly mild and manageable with steroids in patients receiving immune checkpoint inhibitors, highlighting the importance of effective management strategies as these therapies become more widely used.
The study outlines a comprehensive 3-pronged strategy for managing irAEs, including a dedicated Immune Wellness Clinic for monitoring at-risk patients, a repository for supporting research, and an Immunotoxicity Tumor Board for handling severe cases, which can enhance patient care and safety.
Optimizing Care for Patients With Adverse Events From Immunotherapeutics.Sheehan, K., Price, C., Hafez, N.[2021]
Immune checkpoint inhibitors, such as those targeting CTLA-4, PD-1, and PD-L1, have become significant in cancer immunotherapy, showing promise in enhancing antitumor effects through both single-agent and combination therapies.
However, these therapies can lead to immune-related adverse events (irAEs), which vary in frequency and severity, highlighting the need for better understanding and management strategies for these side effects.
Immune-Related Adverse Events From Immune Checkpoint Inhibitors.Marrone, KA., Ying, W., Naidoo, J.[2022]
Immune checkpoint antibodies targeting the PD-1/PD-L1 pathway have shown significant antitumor activity and have been approved for use as single-agent therapies in metastatic malignant melanoma and nonsmall-cell lung cancer.
Understanding the toxicities associated with PD-1/PD-L1 blockade and having effective management strategies is crucial for maximizing both the safety and efficacy of these treatments.
Toxicities of the anti-PD-1 and anti-PD-L1 immune checkpoint antibodies.Naidoo, J., Page, DB., Li, BT., et al.[2023]

Citations

Study Details | NCT04503265 | A Trial of AMXI-5001 for ...ATLAS-101 is a Phase I/II clinical trial of AMXI-5001 in adult participants with advanced malignancies who have previously failed other therapies.
AMXI-5001, a novel dual parp1/2 and microtubule ...Following a 3 days treatment, AMXI-5001 resulted in a robust cytotoxicity in a wide variety of human cancer cell lines (110 lines) of various origins, with very ...
A Trial of AMXI-5001 for Treatment in Patients With ...ATLAS-101 is a Phase I/II clinical trial of AMXI-5001 in adult participants with advanced malignancies who have previously failed other ...
AMXI-5001 for Advanced CancersThis trial is for adults with advanced cancers like ovarian, prostate, pancreatic, or breast cancer that have worsened despite standard treatments. Participants ...
A Trial Of AMXI-5001 For Treatment In Patients With ...ATLAS-101 is a Phase I/II clinical trial of AMXI-5001 in adult participants with advanced malignancies who have previously failed other therapies.
A Trial of AMXI-5001 for Treatment in Patients With Advanced ...ATLAS-101 is a Phase I/II clinical trial of AMXI-5001 in adult participants with advanced malignancies who have previously failed other therapies.
681TiP A phase I/II, open label, multi- ...This study is an open-label, multi-center, non-randomized dose escalation study of AMXI-5001 as monotherapy in patients with refractory advanced.
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