Development Plan

The clinical development plan for inodiftagene vixteplasmid (BC-819) consists of two clinical studies that together constitute a straightforward pathway to potential approval. The CODEX Trial is open for enrollment (click here)

 

The two trials provide independent routes to potential approval in two separate (but related) indications.

The treatment scheme for NMIBC patients is illustrated below. There are two areas of substantial unmet need for patients as they progress through the algorithm of surgical and medical therapy with BCG. We are planning trials in both of these indications.

The Codex study is a single arm trial for registration. It will enroll approximately 140 patients with NMIBC who have been treated with two courses of BCG, who experienced subsequent tumor recurrence; this population is considered to have BCG-unresponsive disease. After resection of tumor, patients will be treated with inodiftagene administered intravesically for two years or until disease recurrence. The primary endpoint of the study is the complete response rate in patients with CIS (v protocol).

Our second registrational trial, the Leo study, is a randomized clinical trial. This study has been granted a Special Protocol Assessment (SPA) by the FDA, a regulatory endorsement that the study design may support approval if it meets its endpoints.

The patient population of the Leo trial is at an earlier stage in their treatment course than in the Codex trial. Patients eligible for Leo will have NMIBC and have been treated with a single course of BCG and suffered recurrence. The study treatment will comprise inodiftagene vixteplasmid and BCG administered together. After resection of recurrent tumor, subjects will be randomized to the combination or to a standard second course of BCG alone. The primary endpoint of this randomized trial is disease free survival.