← Back to searchRecruitingRecruiting
A Trial of AMXI-5001 for Treatment in Patients With Advanced Malignancies
NCT04503265 · AtlasMedx, Incorporated
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
Official title
A Phase I/II, Open Label, Multi-center, Non-randomized Dose Escalation and Dose Expansion Study of AMXI-5001 in Patients With Advanced Malignancies
About this study
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.
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 design
Enrollment target: 122 participants
Allocation: na
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2020-08-12
Estimated completion: 2026-10
Last updated: 2025-05-01
Interventions
Drug: AMXI-5001:Dose Escalation Phase IDrug: AMXI-5001:Dose Expansion Phase II
Primary outcomes
- • Determine the Maximum Tolerated Dose (MTD) (Approximately 12 months)
- • Determine the Recommended Phase 2 Dose (RP2D) for AMXI-5001 as monotherapy (Approximately 12 months)
- • Characterize safety profile of AMXI-5001 (Approximately 24 months)
Sponsor
AtlasMedx, Incorporated · industry
Contacts & investigators
ContactBonnie Wettersten, MS · contact · clinicaltrials@atlasmedx.com · (847) 644-9818
InvestigatorPamela Munster, MD · study_director, AtlasMedx, Incorporated
All locations (4)
University of California, Los Angles (UCLA) Department of Medicine - Hematology/OncologyRecruiting
Los Angeles, California, United States
Johns HopkinsRecruiting
Baltimore, Maryland, United States
SCRI Oncology PartnersRecruiting
Nashville, Tennessee, United States
The University of Texas MD Anderson Cancer CenterRecruiting
Houston, Texas, United States