Lymphoma Clinical Trial
Official title:
An Open-Label, Phase 1, Two-Way, Cross-Over Study of the Effect of the Food on the Pharmacokinetics of MLN8237 (Alisertib) in Patients With Advanced Solid Tumors or Lymphomas
The purpose of this study is to evaluate the effect of food on the single-dose pharmacokinetics (PK) of alisertib administered as an enteric-coated tablet (ECT) formulation in participants with advanced solid tumors or lymphomas.
The drug being tested in this study is called alisertib. Alisertib is being tested in adult
participants with advanced solid tumors or lymphomas.
The study enrolled 26 participants. Participants will be randomly assigned (by chance, like
flipping a coin) to one of the two treatment groups—which will remain undisclosed to the
participant and study doctor during the study (unless there is an urgent medical need):
- Alisertib 50 mg Fed + Fasted
- Alisertib 50 mg Fasted + Fed
All participants will be asked to take one alisertib tablet (ECT), orally, with or without a
standard high-fat breakfast Cycle 1, Day 1, with the respective alternate food intake
condition (fasted to fed or fed to fasted) on Cycle 2, Day 1, each followed by 14-day rest
period. Participants will take alisertib, ECT, orally BID on Days 4 to 10 of Cycles 1 and 2,
each followed by 14-day rest period. From Cycle 3 onwards participants will continue taking
alisertib 50 mg, ECT, orally, BID on Days 1-7, followed by a 14-day rest period in 21-day
cycles until disease progression, occurrence of an unacceptable alisertib-related toxicity.
This multi-center trial conducted at 3 sites in the United States. Participants will make
multiple visits to the clinic and plus a final visit after 30 days of receiving their last
dose of drug for a follow-up assessment.
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