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FDA Approves IND for FP008, a Novel PD-1×IL-10M Fusion Protein for Resistant Solid Tumors

• Fapon Biopharma's FP008, a first-in-class immunocytokine combining anti-PD-1 antibody with engineered IL-10 monomer, receives FDA IND approval for treating solid tumors resistant to anti-PD-1 therapy.

• Preclinical studies demonstrate FP008's ability to counteract T cell exhaustion, increase tumor-infiltrating CD8+ T cells, and enhance immune response while maintaining favorable safety profile.

• The novel therapy shows promise in addressing the significant unmet need for patients with anti-PD-1 resistant solid tumors, with Fapon Biopharma now seeking global partnerships for clinical development.

Fapon Biopharma has achieved a significant milestone with the U.S. Food and Drug Administration's approval of its Investigational New Drug (IND) application for FP008, a pioneering immunocytokine designed for patients with solid tumors who have shown resistance to anti-PD-1 therapy.

Novel Mechanism of Action

FP008 represents an innovative approach to cancer immunotherapy, combining an anti-PD-1 antibody with an engineered IL-10 monomer (IL-10M). This unique fusion protein operates through a dual mechanism: the engineered IL-10M component shows reduced hematologic toxicity, while the anti-PD-1 antibody component enhances IL-10M's therapeutic activity through targeted enrichment and cis-activation.

Promising Preclinical Results

Recent preclinical studies have revealed FP008's remarkable potential in addressing a critical limitation of current PD-1 targeted therapies. While conventional PD-1 antibodies can lead to terminal exhaustion of CD8+ T cells, FP008 effectively counters this process through its IL-10M component. The studies demonstrated several key findings:
  • Significant increase in tumor-infiltrating CD8+ T cells
  • Reduction in terminal exhaustion differentiation of T cells
  • Enhanced production of IFN-γ and GZMB by exhausted CD8+ T cells
  • Favorable safety and pharmacokinetics profile in cynomolgus monkey studies

Clinical Development Strategy

"Global collaboration is central to our vision," says Vincent Huo, President of Fapon Biopharma. The company is actively pursuing strategic partnerships with biopharmaceutical companies worldwide to advance FP008's clinical development and commercialization efforts.

Addressing Unmet Medical Needs

The development of FP008 addresses a significant therapeutic gap in oncology. For patients with solid tumors who have become refractory to anti-PD-1 therapy, treatment options are currently limited. FP008's novel approach could potentially transform the treatment landscape for these patients, offering a new therapeutic strategy when conventional immunotherapies fail.

Technical Development Platform

The creation of FP008 leverages Fapon Biopharma's advanced drug discovery platforms, including:
  • Mammalian cell display technology for antibody discovery
  • Specialized platform for IL-10M fusion protein generation
  • Multispecific antibody development capabilities using Fibody and nanobodies
This technological foundation, combined with the company's end-to-end development capabilities, positions FP008 as a promising candidate in the evolving landscape of cancer immunotherapy.
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