Collagenase Clostridium Histolyticum (CCH)
BiologicalBiologic: Intrafascial injection
Other names: EN3835
NCT Number: NCT06169319
This study will assess the efficacy, safety, and tolerability of 2 different doses of collagenase clostridium histolyticum (CCH) (previously known as EN3835) compared to placebo.
Looking for future studies?
Notify Me18 year–75 year
All sexes
Interventional
Phase 2
Endo Site 8, Tucson, Arizona, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Biologic: Intrafascial injection
Other names: EN3835
Intrafascial injection
Time frame: Baseline, Week 12
Time frame: Baseline, up to Day 85
Time frame: Baseline, up to Day 85
Time frame: Baseline, up to Week 12
Time frame: Baseline, up to Day 85
Time frame: Baseline, up to Day 85
Time frame: Up to Day 85
Time frame: Up to Day 85
Time frame: Up to Day 85
Time frame: Up to Day 85
Time frame: Up to Day 85
Looking for future studies?
Notify MeEndo USA Inc., a Keenova Therapeutics Company
Industry
A Phase 2, Double-blind, Randomized, Placebo-controlled, Dose-ranging Study to Assess the Efficacy, Safety, and Tolerability of EN3835 vs Placebo in the Treatment of Plantar Fasciitis (PFA)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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