Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MC (monocytes control) is an autologous cell therapy consisting of monocytes derived from a patient's own peripheral blood mononuclear cells (PBMC). Developed by Aivita Biomedical, Inc., it serves as the randomized control/placebo arm in Phase 2 clinical trials (such as NCT02033616) evaluating AVOVA-1, an autologous dendritic cell therapy. In these trials, patients with Stage III or IV epithelial ovarian, fallopian tube, or primary peritoneal carcinoma receive either the active dendritic cell treatment or the MC control via subcutaneous injection following standard debulking surgery and primary chemotherapy. The MC control is intended to provide a comparable cellular injection without the specific antigen-loading and maturation processes applied to the active treatment arm, allowing for a double-blind assessment of overall survival and disease progression.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on MC.