A Study in Healthy Subjects to Assess Bioavailability (Proportion of a Drug Which Enters the Circulation to Have an Active Effect) of Acalabrutinib Tablet and Protonpump Inhibitor Effect (Members of a Class of Medications That Inhibits in Gastric Acid Production) for Rabeprazole

PHASE1CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

October 12, 2020

Primary Completion Date

December 11, 2020

Study Completion Date

December 11, 2020

Conditions
Mantle Cell LymphomaCOVID-19
Interventions
DRUG

Acalabrutinib Treatment A

Participants will receive 100 mg AT suspension in water via NG tube.

DRUG

Acalabrutinib Treatment B

Participants will receive 100 mg acalabrutinib capsule suspension via NG tube.

DRUG

Acalabrutinib Treatment C

Participants will receive 100 mg AT suspension in water via NG administration plus 20 mg rabeprazole.

DRUG

Acalabrutinib Treatment D

Participants will receive 100 mg AT orally.

Trial Locations (1)

14050

Research Site, Berlin

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY