WHO ICTRP trial

A study in healthy volunteers to assess the different formulations (recipes) of…

ISRCTN12868063 · International Standard Randomised Controlled Trial Number (ISRCTN) · Not Recruiting

Key facts

Trial ID ISRCTN12868063
Public title A study in healthy volunteers to assess the different formulations (recipes) of the drug product (alectinib)
Scientific title Single part, open-label, phase 1 study designed to evaluate the relative bioavailability of oral alectinib formulations compared with an oral reference alectinib capsule, in healthy subjects
Primary sponsor Chugai Pharmaceutical Co., Ltd.
Registry International Standard Randomised Controlled Trial Number (ISRCTN)
Recruitment status Not Recruiting
Study type Interventional
Phase Phase I
Countries United Kingdom;England
Conditions Cancer Cancer
Interventions Participants will receive a single oral 600 mg dose of one of the following across six study periods: 1. Reference alectinib capsule in the fasted state 2. Alectinib powder for oral suspension in the fed or fasted state 3. Alectinib oral…
Registration date Jul 10, 2022
Target size 26
Secondary IDs 2021-003298-78;Nil known;JP43290, IRAS 301567
Registry page isrctn.com

At a glance

  • No Results available

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

Browse all WHO ICTRP trial registrations