🇺🇸 FDA
Pipeline program

KENACORT 40 mg/ml sospensione iniettabile, Suero Fisiológico Braun 0,9% disolvente para uso parenteral Cloruro de sodio, Lidocaína B. Braun 20 mg/ml solución inyectable, BUPIVACAÍNA PHYSAN 0,25% SOLUCIÓN INYECTABLE

TRAPEZIUS

Approved small_molecule active

Quick answer

KENACORT 40 mg/ml sospensione iniettabile, Suero Fisiológico Braun 0,9% disolvente para uso parenteral Cloruro de sodio, Lidocaína B. Braun 20 mg/ml solución inyectable, BUPIVACAÍNA PHYSAN 0,25% SOLUCIÓN INYECTABLE for TRAPEZIUS MYOFASCIAL SYNDROME IN FIBROMYALGIA PATIENTS is a Approved program (small_molecule) at The George Institute with 1 ClinicalTrials.gov record(s).

Program details

Company
The George Institute
Indication
TRAPEZIUS MYOFASCIAL SYNDROME IN FIBROMYALGIA PATIENTS
Phase
Approved
Modality
small_molecule
Status
active

Clinical trials