Phase I Dose Escalation Study of Intravenously Administered S64315 in Combination With Orally Administered Venetoclax in Patients With Acute Myeloid Leukaemia.

PHASE1CompletedINTERVENTIONAL
Enrollment

37

Participants

Timeline

Start Date

November 28, 2018

Primary Completion Date

November 12, 2022

Study Completion Date

May 30, 2023

Conditions
Acute Myeloid Leukaemia
Interventions
COMBINATION_PRODUCT

S 64315 (also referred as MIK665) and venetoclax

"The treatment combination period can only begin after the planned dose of venetoclax is reached. Depending on the administration dosing schedule, the combination treatment at the planned doses may be preceded by a 2-week Lead-In Dose period of S64315 (fixed dose) during which the patient continues to receive venetoclax daily. Once the planned dose of both drugs is reached the schedule will be a 21-day cycle with a weekly regimen for S64315 and a daily regimen for venetoclax.~S64315 should be administered 2 to 4 hours after venetoclax intake, via IV infusion. The dose escalation will start at 50 mg once a week and doses up to 250 mg once a week might be explored.~Venetoclax will be administered orally once a day. The dose escalation will start at 100 mg daily and doses up to 600 mg daily might be explored. Venetoclax must be taken with a meal (ideally during breakfast) in order to avoid reduced efficacy."

Trial Locations (7)

77030

The University of Texas MD Anderson Cancer Center, Houston, TX, Houston

06511

Smilow Cancer Hospital at Yale, New Haven

Unknown

Peter MacCallum cancer centrer, Melbourne

The Alfred Hospital Department of Haematology, Victoria Park

Institut Paoli-Calmettes, Marseille

Hopital Saint-Antoine, Paris

Institut Universitaire du Cancer Toulouse - Oncopole, Toulouse

All Listed Sponsors
collaborator

ADIR, a Servier Group company

INDUSTRY

lead

Institut de Recherches Internationales Servier

OTHER

NCT03672695 - Phase I Dose Escalation Study of Intravenously Administered S64315 in Combination With Orally Administered Venetoclax in Patients With Acute Myeloid Leukaemia. | Biotech Hunter | Biotech Hunter