Study Details

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A study to investigate the effect of hepatic impairment on the pharmacokinetics, safety and tolerability of ASP2215

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT02571816

Astellas Study ID

The unique identification code given by the study sponsor.

2215-CL-0106

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

N/A

Follow Trial

Condition

Liver Disease, Healthy Volunteer

Phase

These clinical trials are usually the first time an experimental treatment is studied in a small group of people.

Phase 1

Age

18 years - 75 years

Sex

Female & Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Oct 2015 - Mar 2016

Masking

None (Open Label)

Enrollment number

24

A Phase 1 study to investigate the effect of hepatic impairment on the pharmacokinetics, safety and tolerability of ASP2215

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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Locations

Site US10001

Miami, United States, 33014

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