Drug intelligence / Profile preview

CV8102 + anti-PD-1

Development stage
Unknown
Lead developer
CureVac
Modality
MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intratumoral, Intravenous
01

Overview

CV8102 + anti-PD-1 is a combination immunotherapy regimen under clinical investigation for the treatment of advanced solid tumors, particularly melanoma, cutaneous squamous cell carcinoma, head and neck squamous cell carcinoma, and adenoid cystic carcinoma. CV8102 is a synthetic single-stranded, non-coding RNA complexed with a cationic peptide that acts as an agonist of toll-like receptor 7/8 (TLR7/8) and retinoic acid-inducible gene I (RIG-I), thereby activating both innate and adaptive immune responses within the tumor microenvironment. When administered intratumorally, CV8102 stimulates local immune activation and enhances infiltration of T cells into tumors. The addition of systemic anti-programmed death protein 1 (PD-1) antibody therapy further boosts antitumor immunity by blocking PD-1-mediated inhibition of T cells. Preclinical studies have shown synergistic effects between these agents, leading to improved tumor control compared to either agent alone. Early-phase clinical trials indicate that this combination is generally well tolerated with preliminary evidence of efficacy in patients who are refractory or naïve to prior PD-1 inhibitor therapy[3][5][4][6].

02

Targets

TLR8 (Toll-like receptor 8)TLR7 (Toll-like receptor 7)PDCD1 (Programmed cell death protein 1 receptor)

Beyond the preview

Go deeper on CV8102 + anti-PD-1.

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 CV8102 + anti-PD-1.

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