LivingGLP1
Study S002051

A Phase 2a Dose-Finding Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of NLY01, a PEGylated Exenatide, When Administered as a Single Dose in Subjects With Type 2 Diabetes

Registration

Registration
NCT04159766
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
20
Start
2019-10-16
Primary completion
2020-12-04
Lead sponsor
Neuraly, Inc.
Conditions
Type2 Diabetes; Diabetes Mellitus, Type 2
Interventions
DRUG:NLY01; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Number of participants with Treatment Emergent Adverse Events [35 days]
  • Number of Incidences of Adverse Events [35 days]
  • Plasma glucose [24 hours]
  • Change in serum insulin [24 hours]
  • Change in plasma glucagon [24 hours]

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