drugset / Trial / NCT06115512

A Phase 3 Study of AGA111 in Patients With Degenerative Disc Disease Undergoing Lumbar Interbody Fusion

NCT06115512 ↗

Phase 3 Terminated 412 enrolled Angitia Biopharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of the study is to assess the overall efficacy of a single intervertebral local administration of AGA111 in patients with degenerative disc disease undergoing lumbar interbody fusion.

Timeline

Start
2023-12-08
Primary completion
2025-11-28
Completion
2026-06-12

Outcome

Outcome not reported

Stopped (Business): “Sponsor's strategic decision not related to safety concerns.”

Drugs

EvaluationDrugModalityDoseRoute
Subject AGA111 Unknown — Other