Drug intelligence / Profile preview

NEO-PV-01 + poly-ICLC + nivolumab + ipilimumab

Development stage
Unknown
Lead developer
Dana-Farber Cancer Institute
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Vaccines & Immunotherapeutics
Administration
Intravenous (nivolumab, Ipilimumab), Subcutaneous Or Intradermal (NEO-PV-01 + poly-ICLC)
01

Overview

**NEO-PV-01 + poly-ICLC + nivolumab + ipilimumab** is an experimental multi-agent immunotherapy regimen for cancer. It combines: - **NEO-PV-01**: a personalized neoantigen peptide vaccine individually manufactured for each patient based on tumor-specific genetic mutations. It is designed to induce strong, specific T cell immune responses against tumor cells[1][3][5]. - **poly-ICLC**: an immune adjuvant and synthetic double-stranded RNA (Hiltonol), which boosts the vaccine's immunogenicity by stimulating innate immune receptors, such as toll-like receptor 3, enhancing anti-tumor immunity[3][5]. - **nivolumab**: a human IgG4 monoclonal antibody that inhibits programmed cell death protein 1 (PD-1), blocking its signaling and boosting T cell responses against tumor cells[2][3][5][6]. - **ipilimumab**: a monoclonal antibody blocking cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), removing an inhibitory checkpoint to strengthen T cell activation[2][4][5][6]. This combination is intended to produce robust, multi-modal anti-tumor immune activation: the vaccine primes neoantigen-specific immune reactions, poly-ICLC boosts the vaccine effect, and checkpoint inhibitors (nivolumab and ipilimumab) lift immune suppression, maximizing T cell–mediated tumor destruction. Clinical trials have evaluated this regimen primarily in advanced melanoma, as well as bladder cancer and lung cancer[3][5][7].

Other names
Hiltonol (poly-ICLC)
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)pMHC-I (Peptide–MHC class I complex)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)TLR3 (Toll-like receptor 3)

Beyond the preview

Go deeper on NEO-PV-01 + poly-ICLC + nivolumab + ipilimumab.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Clinical trials

Full profile access

Follow clinical development from study design and recruitment through results.

  • Trial phase
  • Status
  • Readouts

Indications & development

Full profile access

Explore development by indication, patient population, and geography.

  • Indications
  • Development status
  • Countries

Licensing & deals

Full profile access

Trace asset ownership, licensing agreements, and commercial partnerships.

  • Partners
  • Deal terms
  • Milestones

Patents & exclusivity

Full profile access

Explore the patent landscape and regulatory exclusivity around an asset.

  • Patents
  • Expiration dates
  • Exclusivity

Competitive landscape

Full profile access

Compare development programs by target, modality, and indication.

  • Competing assets
  • Targets
  • Development stage

Research & analysis

Full profile access

Connect source evidence and development news to your research questions.

  • Publications
  • News
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on NEO-PV-01 + poly-ICLC + nivolumab + ipilimumab.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call