LivingGLP1
Study S001334

A Phase I/II Proof of Concept, Open-Label, Repeat Dose, Dose Escalation Study of NM-002 in Adult Patients With Short Bowel Syndrome (SBS)

Registration

Registration
NCT04379856
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1; PHASE2
Masking
NONE
Status
UNKNOWN
Enrollment
12
Start
2020-06-23
Primary completion
2020-12-11
Lead sponsor
9 Meters Biopharma, Inc.
Conditions
Short Bowel Syndrome
Interventions
DRUG:NM-002
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • To assess the safety and tolerability of repeated doses of NM002 three different dose levels [56 days]

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