A Trial of AMXI-5001 for Treatment in Patients With Advanced Malignancies
Conditions
Advanced Malignant Neoplasm, Breast Cancer, Ovarian Cancer, Homologous Recombination Deficiency, Prostate Cancer, Pancreatic CancerDrugs
AMXI-5001:Dose Escalation Phase I, AMXI-5001:Dose Expansion Phase IISummary
ATLAS-101 is a Phase I/II clinical trial of AMXI-5001 in adult participants with advanced malignancies who have previously failed other therapies. The study has two phases. The purpose of Phase I (Dose Escalation) is to confirm the appropriate treatment dose and Phase II (Dose Expansion) is to characterize the safety and efficacy of AMXI-5001.
Detailed Description
AMXI-5001 is an orally available dual PARP (poly adenosine diphosphate [ADP] ribose polymerase) and microtubule polymerization inhibitor. ATLAS-101 is a Phase I/II, open label, multi-center, non-randomized Dose Escalation and Dose Expansion study in participants with advanced malignancies. Study enrollment is approximately 122 participants. All participants receive oral AMXI-5001, twice daily, as monotherapy. Following Phase I (Dose Escalation) to identify the Maximum Tolerated Dose and the Recommended Dose for use in Phase II, additional participants will be enrolled into the Dose Expansion Phase to further characterize the safety, pharmacology, and clinical efficacy of AMXI-5001.
Locations
4 locations Found with status Recruiting
Status
- RECRUITING
Central Contacts
- Bonnie Wettersten, MS
- (847) 644-9818
- [email protected]
Study Director
- Pamela Munster, MD
Status
- RECRUITING
Central Contacts
- Bonnie Wettersten, MS
- (847) 644-9818
- [email protected]
Study Director
- Pamela Munster, MD
Status
- RECRUITING
Central Contacts
- Bonnie Wettersten, MS
- (847) 644-9818
- [email protected]
Study Director
- Pamela Munster, MD
Status
- RECRUITING
Central Contacts
- Bonnie Wettersten, MS
- (847) 644-9818
- [email protected]
Study Director
- Pamela Munster, MD
Eligibility Criteria
Inclusion Criteria (Key Factors):
1. Has pathologically confirmed advanced or metastatic malignancy characterized by one or more of the following:
1. Patient is intolerant of existing therapy(ies) known to provide clinical benefit for their condition
2. Malignancy is refractory to existing therapy(ies) known to potentially provide clinical benefit
3. Malignancy has progressed after standard therapy
2. Has evaluable or measurable tumor(s) in dose escalation by standard radiological and/or laboratory assessments as applicable to their malignancy.
3. Eastern Co-operative Oncology Group (ECOG) PS 0-1
4. Participant must be 18 years of age or older
5. Able to understand and sign consent
Exclusion Criteria (Key Factors):
1. Receiving cancer treatment at the time of enrollment
2. Any clinically significant disease or condition affecting a major organ system
3. Significant cardiovascular disease or electrocardiogram (ECG) abnormalities
4. Use of a strong inhibitor or inducer of CYP3A4 within 7 days prior to start of study therapy and throughout the study (e.g., some antibiotics, antifungals, anticonvulsants, grapefruit)
5. Has had a previous (within 2 years) or has a current malignancy other than the target cancer
Study Plan
AMXI-5001 Treatment
EXPERIMENTAL
Single Arm Study, all participants will receive AMXI-5001.
DRUG:
AMXI-5001:Dose Escalation Phase IDescription:
Phase I will enroll up to 70 participants to identify the Recommended Phase II daily dose in the treatment of various cancers and to characterize the safety, pharmacology, and clinical efficacy of AMXI-5001. AMXI-5001 is administered orally twice daily, with food. AMXI-5001 is administered weekly on a continuous 7-day schedule. Each cycle is 28 days.DRUG:
AMXI-5001:Dose Expansion Phase IIDescription:
Phase II will enroll up to 52 study participants to further characterize the safety, pharmacology, and clinical efficacy of AMXI-5001. AMXI-5001 is administered orally twice daily, with food. AMXI-5001 is administered weekly on a continuous 7-day schedule. Each cycle is 28 days.
Outcome Measures
Primary Outcome Measures
Determine the Maximum Tolerated Dose (MTD)
Determine the Recommended Phase 2 Dose (RP2D) for AMXI-5001 as monotherapy
Characterize safety profile of AMXI-5001
Secondary Outcome Measures
Measure concentration of AMXI-5001 in plasma samples
Determine change in anti-tumor activity following administration of AMXI-5001
Timeline
Last Updated
December 10, 2024Start Date
August 7, 2020Today
May 12, 2025Completion Date ( Estimated )
October 1, 2026
Sponsors of this trial
Lead Sponsor
AtlasMedx, Incorporated