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Scientific visualization of a compact nanobody approaching a cancer cell membrane

Novel therapeutic nanobody

Reactivates p53 functionality. Destroys cancer.

PHP Biotech is developing PHP53-nb, a first-in-class humanized camelid nanobody designed to enter tumor cells, restore mutant p53 function, and trigger apoptosis in aggressive solid tumors — beginning with triple-negative breast cancer.

~50%

of all human cancers carry a TP53 mutation

~70%

of aggressive tumors contain a TP53 mutation

2.4M

women diagnosed with breast cancer worldwide in 2024

~17 kDa

molecular weight of PHP53-nb — about 1/10th a monoclonal antibody

Our focus

Targeting the most aggressive cancers

Triple-negative breast cancer is highly aggressive, with fewer targeted options than other breast-cancer subtypes. PHP53-nb is a patented, linker-free nanobody that internalizes within cancer cells and initiates reactivation of p53, leading to apoptosis.

The World Health Organization estimates 2.4 million women were diagnosed with breast cancer in 2024, with 694,000 deaths globally. Mutations in TP53 — present in about half of all human cancers — remain among the most important and least successfully drugged oncology targets.

Fluorescence microscopy of a tumor organoid in teal and magenta channels
Conceptual microscopy of tumor biology. PHP53-nb remains investigational.

Mechanism of action

PHP53-nb specifically targets cancer cells — then goes inside.

  1. 01

    Selective tumor binding

    PHP53-nb preferentially engages a tumor-associated membrane ligand, supporting selectivity for biologically defined tumor subpopulations rather than unselected tissue.

  2. 02

    Endocytosis

    The nanobody enters the cell through clathrin-coated vesicles — a first-in-class intracellular biologic route for this payload — rather than remaining at the cell surface.

  3. 03

    Cytoplasmic release

    After internalization, PHP53-nb leaks into the cytoplasm, where the genetically integrated 3-NAntC peptide can act without chemical linkers or conjugation steps.

  4. 04

    Stress and p53 reactivation

    Proteasome modulation, rising reactive oxygen species, and endoplasmic reticulum stress trigger the unfolded protein response and restore p53 apoptotic signaling.

  5. 05

    Mitochondrial collapse

    Mitochondrial permeabilization follows, committing the cancer cell to apoptosis while benign control lines in published summaries remain comparatively spared.

Studio render of a compact single-domain nanobody protein

Platform

Smaller than an antibody. Built for the inside of a cell.

At ~17 kDa, PHP53-nb is about one-tenth the size of a traditional monoclonal antibody. The 3-NAntC peptide is genetically integrated into the GEN01-AD nanobody — no chemical linkers — enabling a modular intracellular biologic platform.

TraitNanobodymAb
Molecular weight~17 kDa~150 kDa
Tumor penetrationDeeperLimited
StabilityHigherLower
Production costLowerHigher

Pipeline

One lead. A reusable engine.

Full pipeline

Preclinical

PHP53-nb

Therapeutic humanized camelid nanobody

Lead candidate. Preclinical package advancing toward planned IND-enabling work, with Phase I anticipated in 2027.

Integrated

3-NAntC

p53-reactivating peptide payload

Genetically engrafted into the nanobody scaffold — no linkers, post-modifications, or extra manufacturing steps.

Platform

GEN01-AD

Humanized camelid nanobody delivery platform

Reusable architecture for additional payloads beyond PHP53-nb, including future multi-specific constructs.

About

A team of dedicated experts pushing what is possible in cancer treatment.

Founded in 2020 by healthcare entrepreneurs and powered by a scientific team, global CROs, and CDMOs specializing in nanobody and translational biotechnology. Headquartered in Southlake, Texas.

  • First-in-class humanized nanobody with a novel intracellular mechanism
  • Encouraging preclinical selectivity, tolerability, and tumor retention
  • CHO-based manufacturing with 100-fold yield gains from gene optimization
Scientists working in a modern biotechnology laboratory

Questions people ask

What is PHP Biotech?+

PHP Biotech International Inc. is a US-based, privately held biotechnology company founded in 2020 and headquartered in Southlake, Texas. It develops intracellular nanobody therapeutics designed to restore p53 apoptotic function in aggressive solid tumors, starting with triple-negative breast cancer.

What is PHP53-nb?+

PHP53-nb is PHP Biotech’s lead candidate: a first-in-class humanized camelid nanobody that genetically incorporates the p53-reactivating peptide 3-NAntC. It is engineered to enter tumor cells, reactivate mutant p53, and trigger apoptosis. It is investigational and not approved by the FDA.

How does PHP53-nb work?+

PHP53-nb binds a tumor-associated membrane ligand, enters the cell by endocytosis, and releases its payload in the cytoplasm. That payload drives oxidative and ER stress, reactivates p53 signaling, collapses mitochondria, and commits the cancer cell to programmed death.

What is a nanobody?+

A nanobody is a single-domain antibody fragment derived from camelid heavy-chain antibodies. At about 17 kDa, PHP53-nb is roughly one-tenth the size of a traditional monoclonal antibody (~150 kDa), which can improve tumor penetration, stability, and manufacturing economics.

What is p53 and why does it matter in cancer?+

p53 is a tumor-suppressor protein often called the guardian of the genome. Mutations in TP53, the gene that encodes p53, occur in about half of all human cancers and in a still higher share of aggressive tumors. Restoring p53 function is a long-sought, historically difficult oncology strategy.

Read the full FAQ

Morning light through laboratory glassware

Partner on a new modality for undruggable pathways.

Scientific collaborators, CROs, CDMOs, and qualified investors are invited to start a conversation.