Covance Clinical Research Unit Ltd
Leeds, Yorkshire, LS2 9LH, United Kingdom
NCT Number: NCT02361034
This is a multiple Ascending dose (MAD) study with GRC 27864 in Healthy and Elderly Subjects.
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Notify Me18 year–55 year
All sexes
Interventional
Phase 1
Leeds, Yorkshire, LS2 9LH, United Kingdom
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Baseline upto 42 days after administration of the study drug.
Time frame: Predose and postdose from 0.25 to 48 hrs and from Day 1 to day 28
Time frame: Predose and postdose from 0.25 to 48 hrs and from Day 1 to day 28
Time frame: Predose and postdose from 0.25 to 48 hrs and from Day 1 to day 28
Time frame: Predose and postdose from 0.25 to 48 hrs and from Day 1 to day 28
Time frame: Predose and postdose from 0.25 to 48 hrs and from Day 1 to day 28
Time frame: Predose and postdose from 0.25 to 48 hrs and from Day 1 to day 28
Time frame: Predose and postdose from 0.25 to 48 hrs and from Day 1 to day 28
Time frame: 6 hours, and 24 hours postdose on Day 26
Glenmark Pharmaceuticals S.A.
Industry
A Two-Part, Phase I Study of Orally Administered GRC 27864, a Novel, Microsomal Prostaglandin E Synthase-1 Enzyme (mPGES-1) Inhibitor, to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple Ascending Doses in Healthy Subjects (Part 1), and of Multiple Doses in Elderly Subjects (Part 2)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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