Geneva, March 23 -- International Clinical Trials Registry received information related to the study (NCT07455955) titled 'Personalized Antiemetic Regimen According to Patients' Pharmacogenetic Profile' on March 3.

Study Type: Interventional

Study Design: Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Single (Participant).

Primary Sponsor: Chinese University of Hong Kong

Condition: Breast Cancer

Intervention: Drug: Standard antiemetic regimen or Olanzapine antiemetic regimen

Recruitment Status: Not recruiting

Phase: Phase 2

Date of First Enrollment: June 3, 2026

Target Sample Size: 200

Countries of Recruitment: Hong Kong

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