Study Investigating STA363 Compared to Placebo in Patients With Chronic Discogenic Low Back Pain

PHASE2UnknownINTERVENTIONAL
Enrollment

110

Participants

Timeline

Start Date

July 31, 2020

Primary Completion Date

September 1, 2023

Study Completion Date

October 31, 2023

Conditions
Discogenic Pain
Interventions
DRUG

STA363 containing 90 mg (60 mg/mL) lactic acid

STA363 (90 mg) will be injected into maximally two pain-generating degenerated intervertebral discs

DRUG

STA363 containing 180 mg (120 mg/mL) lactic acid

STA363 (180 mg) will be injected into maximally two pain-generating degenerated intervertebral discs

DRUG

Placebo

Placebo will be injected into maximally two pain-generating degenerated intervertebral discs

Trial Locations (17)

Unknown

Alrijne Ziekenhuis Leiderdorp, Leiderdorp

Rijnstate Hospital Anesthesiology and Pain, Velp

Belgorod Regional Clinical Hospital of Saint Joasaph, Belgorod

Regional Clinical Hospital #3, Chelyabinsk

Kirov State Medical University, Kirov

Ochapovsky Regional Clinical Hospital #1, Krasnodar

Krasnoyarsk Interdistrict Clinical Emergency Hospital, Krasnoyarsk

Siberian Research Clinical Center, Krasnoyarsk

Privolzhsky Research Medical University, Nizhny Novgorod

Bekhterev Psychiatry and Neurology Center, Saint Petersburg

LLC MART, Saint Petersburg

Smolensk Regional Clinical Hospital, Smolensk

Tula Regional Clinical Hospital, Tula

Hospital Quirónsalud Córdoba, Córdoba

Complejo Hospitalario Ruber Juan Bravo, Madrid

Hm Puerta Del Sur, Móstoles

Hospital Universitario Quirónsalud Madrid, Pozuelo de Alarcón

Sponsors
All Listed Sponsors
lead

Stayble Therapeutics

INDUSTRY

NCT04673461 - Study Investigating STA363 Compared to Placebo in Patients With Chronic Discogenic Low Back Pain | Biotech Hunter | Biotech Hunter