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Study to Evaluate Safety of C-1101 Versus Sterile Saline in Adults With Chronic Painful Lumbosacral Radiculopathy

NCT07264270 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2026-03-17

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and tolerability of C-1101 administered as a single dose, transforaminal epidural injection compared to sterile saline

Conditions

  • Lumbosacral Radicular Pain
  • Sciatic Radiculopathy
  • Sciatic Leg Pain
  • Sciatica
  • Lumbosacral Radicular Syndrome
  • Lumbosacral Radiculopathy

Interventions

DRUG

C-1101

C-1101

OTHER

Placebo: Sterile Saline

Placebo

Sponsors & Collaborators

  • Consano Bio

    lead INDUSTRY

Principal Investigators

  • Consano Chief Medical Officer · Consano Bio

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-12-03
Primary Completion
2026-11-01
Completion
2026-12-01

Countries

  • Australia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07264270 on ClinicalTrials.gov