Study identifier:D5680C00002
ClinicalTrials.gov identifier:NCT03755934
EudraCT identifier:2018-002523-42
CTIS identifier:N/A
A Randomised, Double-Blind, Placebo-Controlled, Dose-Response Study of the Efficacy and Safety of MEDI7352 in Subjects with Painful Diabetic Neuropathy
Painful Diabetic Neuropathy
Phase 2
No
MEDI7352
All
112
Interventional
18 Years - 80 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Aug 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Placebo Comparator: Placebo Participants received 6 doses of intravenous (IV) placebo infusion matched to MEDl7352 during 12-week treatment period. | Other: Placebo Participants will receive IV infusion of placebo as stated in arm description. |
Experimental: MEDl7352 Low Dose Participants received 6 doses of IV MEDl7352 low dose during 12-week treatment period. | Drug: MEDI7352 Participants will receive IV infusion of MEDI7352 as stated in arm description. |
Experimental: MEDl7352 Medium Dose Participants received 6 doses of IV MEDl7352 medium dose during 12-week treatment period. | Drug: MEDI7352 Participants will receive IV infusion of MEDI7352 as stated in arm description. |
Experimental: MEDI7352 High Dose Participants received 6 doses of IV MEDl7352 high dose during 12-week treatment period. | Drug: MEDI7352 Participants will receive IV infusion of MEDI7352 as stated in arm description. |