Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**SV-102** is an investigational intratumoral fixed-dose, multi-target immunotherapy developed by Syncromune for metastatic castration-resistant prostate cancer. The drug comprises four active components: an anti-PD-1 monoclonal antibody, an anti-CTLA-4 monoclonal antibody, a CD40 agonist monoclonal antibody, and a CpG oligodeoxynucleotide TLR9 agonist. In the SYNC-T treatment approach, SV-102 is infused directly into a partially cryoablated tumor to combine locally released patient-specific tumor antigens with checkpoint blockade and innate and adaptive immune stimulation, with the aim of generating a systemic antitumor T-cell response. SV-102 has FDA Fast Track designation for metastatic castration-resistant prostate cancer and is being evaluated in the Phase 2 LEGION-100 study. ([syncromune.com](https://syncromune.com/2024/07/01/syncromune-granted-fda-fast-track-designation-for-sync-t-sv-102-for-the-treatment-of-metastatic-castrate-resistant-prostate-cancer-mcrpc/))
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 SV-102.