Drug intelligence / Profile preview

AdC68 + plasmid DNA + tremelimumab + PF-06801591

Development stage
Unknown
Lead developer
Pfizer
Modality
Adenoviral Vectors → Other Viral Vectors → Viral Vectors → Gene Addition/Replacement → Gene Therapies, Plasmid DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Subcutaneous, Intratumoral (for Viral Vector/plasmid Dna Modalities Depending On Protocol)
01

Overview

This is a combination investigational therapy comprising four components: - **AdC68:** A chimpanzee-derived adenoviral vector (chimpanzee adenovirus serotype 68), engineered for use either as a vaccine delivery vehicle or gene therapy platform in cancer therapy. AdC68 vectors are notable for low human seroprevalence and capacity to elicit strong cellular and humoral immune responses[7][9]. - **plasmid DNA:** Used in combination with AdC68 to deliver genes encoding tumor-associated antigens, immune-stimulatory proteins, or other therapeutic sequences, acting as a gene therapy or vaccination strategy against cancer. - **tremelimumab:** A fully human monoclonal antibody targeting Cytotoxic T-Lymphocyte Associated Protein 4 (CTLA-4), functioning as a checkpoint inhibitor that blocks inhibitory signaling in T lymphocytes, resulting in enhanced antitumor immune activity. - **PF-06801591 (sasanlimab):** A monoclonal antibody targeting programmed death-1 (PD-1) receptor, functioning as an immune checkpoint inhibitor by preventing PD-1 interaction with its ligands and thus releasing inhibitory immune signals in the tumor microenvironment[2][4][6][10]. This combination is being investigated for synergistic immune activation: the gene therapy and viral vector prime and boost the immune response against tumor antigens, while the dual checkpoint blockade (tremelimumab and PF-06801591) further amplifies T cell-mediated antitumor effects. The primary, but not exclusive, indication is advanced malignancies, especially solid tumors (notably non-small cell lung cancer and urothelial carcinoma in referenced clinical trials for PF-06801591)[2][8][10].

Other names
AdC68 + plasmid DNA + tremelimumab + PF-06801591
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)PSCA (Prostate stem cell antigen)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)

Beyond the preview

Go deeper on AdC68 + plasmid DNA + tremelimumab + PF-06801591.

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 AdC68 + plasmid DNA + tremelimumab + PF-06801591.

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