Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
mRNA-transfected dendritic cell vaccine (Inge Marie Svane) is an autologous cell-based cancer immunotherapy developed for the treatment of metastatic castration-resistant prostate cancer (mCRPC). The vaccine is produced by harvesting a patient's monocytes via leukapheresis, which are then matured ex vivo into dendritic cells using a cytokine cocktail including GM-CSF, IL-4, IL-1β, TNFα, IL-6, and PGE2. These mature dendritic cells are subsequently transfected with messenger RNA (mRNA) encoding four specific tumor-associated antigens: Prostate-Specific Antigen (PSA), Prostatic Acid Phosphatase (PAP), survivin, and human Telomerase Reverse Transcriptase (hTERT). Once administered intradermally, these dendritic cells present the antigens to the patient's immune system to stimulate a targeted T-cell response against prostate cancer cells. This therapeutic approach has been investigated in Phase II clinical trials, often in combination with standard chemotherapy such as docetaxel, to evaluate its ability to induce immune responses and improve clinical outcomes in patients with advanced prostate cancer.
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 mRNA-transfected dendritic cell vaccine (Inge Marie Svane).