Title
A Trial of AMXI-5001 for Treatment in Patients With Advanced Malignancies
A Phase I/II, Open Label, Multi-center, Non-randomized Dose Escalation and Dose Expansion Study of AMXI-5001 in Patients With Advanced Malignancies
Phase
Phase 1/Phase 2Lead Sponsor
AtlasMedx, IncStudy Type
InterventionalStatus
RecruitingIntervention/Treatment
AMXI-5001:Dose Escalation Phase I AMXI-5001:Dose Expansion Phase IIStudy Participants
122ATLAS-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.
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.
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.
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.
Single Arm Study, all participants will receive AMXI-5001.
Inclusion Criteria (Key Factors): Has pathologically confirmed advanced or metastatic malignancy characterized by one or more of the following: Patient is intolerant of existing therapy(ies) known to provide clinical benefit for their condition Malignancy is refractory to existing therapy(ies) known to potentially provide clinical benefit Malignancy has progressed after standard therapy Has evaluable or measurable tumor(s) in dose escalation by standard radiological and/or laboratory assessments as applicable to their malignancy. Eastern Co-operative Oncology Group (ECOG) PS 0-1 Participant must be 18 years of age or older Exclusion Criteria (Key Factors): Receiving cancer treatment at the time of enrollment Any clinically significant disease or condition affecting a major organ system Significant cardiovascular disease or electrocardiogram (ECG) abnormalities 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) Has had a previous (within 2 years) or has a current malignancy other than the target cancer
