A Multinational, Multicenter, Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Activity of FP 045 in Patients with Fanconi Anemia (FusuciA Study)

Description

This is a multi-center, Phase 1/2 study to determine the Optimal Biologic Dose (OBD) and to evaluate the safety, tolerability, PK, and preliminary activity of FP 045 when administered orally in young adult/adolescent and pediatric patients with Fanconi anemia. The study will enroll a total of 4 young adult/adolescent patients and a minimum of 8 and up to 12 pediatric patients with mild-moderate bone marrow failure who have not undergone hematopoietic cell transplant. This makes the total patient number between 12-16 total. Dose escalation will occur individually for each patient, within each age group. Each patient will receive each of 3 dose levels of FP 045 (intra-patient dose escalation), beginning with Dose Level 1, followed by Dose Levels 2 and 3. Each dose level will be administered for 28 days prior to escalation to the next higher dose level for that patient.Dose escalation will begin with young adult/adolescent patients. The initial two patients enrolled in the study will be \

Trial Eligibility

Inclusion Criteria: * male or female aged 3-35 * documented Fanconi anemia by chromosome breakage analysis * females of child-bearing potential and males required to use highly effective birth control * mild to moderate bone marrow failure with at least one cytopenia of \> grade 1 severity Exclusion Criteria: * history of any malignancy except focal squamous cell or basal cell carcinoma of the skin or carcinoma in situ of cervix * has myelodysplastic syndrome or acute leukemia per world health organization (WHO) criteria * has history of any significant medical conditions * has aspartate aminotransferase (AST)/alanine aminotransferase (ALT) \> 5x upper limit of normal (ULN) or calculated creatinine clearance (Clcr) of \< 50 mL/min * has active Hepatitis B or C * has an ongoing systemic infection * requires a strong CYP3A4 inhibitor * has had major surgery within 30 days * Active graft versus host disease requiring systemic treatment * Has a history of bone marrow or stem cell transplant

Study Info

Interventions

Locations Recruiting

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