Curated News
By: NewsRamp Editorial Staff
June 29, 2026

Oncotelic’s Deciparticle Platform Validated for IV Drug Delivery

TLDR

  • Oncotelic's Deciparticle platform could enable intravenous delivery of poorly soluble drugs, giving an edge in drug formulation.
  • The Deciparticle platform uses a cGMP manufacturing process to formulate poorly water-soluble compounds like everolimus for intravenous delivery.
  • Oncotelic's technology aims to improve cancer treatment by enabling safer, more effective delivery of therapeutic drugs.
  • The Deciparticle nanoparticle platform was detailed in a peer-reviewed manuscript in the International Journal of Molecular Sciences.

Impact - Why it Matters

This validation of the Deciparticle platform is important because it addresses a fundamental challenge in drug development: the delivery of hydrophobic, poorly water-soluble compounds. Many promising therapeutics fail due to solubility issues, limiting their effectiveness and patient access. By enabling intravenous delivery of such compounds, this platform could expand the arsenal of treatments for cancer and other diseases, potentially improving outcomes for patients with limited options. The ongoing Phase 1b trial for Sapu003 in mTOR-sensitive tumors represents a tangible step toward clinical application, and the platform's scalability suggests broad future impact across multiple therapeutic areas.

Summary

Oncotelic Therapeutics (OTCQB: OTLC), in collaboration with Sapu Nano, has announced a significant breakthrough: the publication of a peer-reviewed manuscript in the International Journal of Molecular Sciences that validates its proprietary Deciparticle(TM) nanoparticle platform. This platform was used to develop Sapu003, an investigational intravenous everolimus formulation currently in a Phase 1b clinical trial. The publication details the platform's formulation design, scalable cGMP manufacturing process, product stability, and preclinical performance, highlighting its potential to enable intravenous delivery of poorly water-soluble therapeutic compounds. This is a critical advancement because many promising drug candidates suffer from poor solubility, limiting their clinical utility. The Deciparticle(TM) platform could unlock the potential of numerous hydrophobic drugs, expanding treatment options for patients.

The research also supports broader applications for the Deciparticle(TM) platform beyond everolimus, including other hydrophobic drug candidates. Sapu003 is being evaluated in a Phase 1b dose-escalation study in patients with advanced mTOR-sensitive solid tumors, assessing safety, pharmacokinetics, and preliminary antitumor activity in combination with exemestane. Oncotelic Therapeutics, a clinical-stage biopharmaceutical company focused on oncology and immunotherapy, is driving this innovation. The company's CEO, Dr. Vuong Trieu, has over 500 patent applications and 75 issued U.S. patents. Oncotelic also owns 45% of GMP Bio, a joint venture advancing its own pipeline, and develops PDAOAI, a proprietary AI platform for drug discovery and manufacturing. The company's relationship with SAPU Bio, an OEB-5 sterile injectable cGMP manufacturing facility, further supports the platform's development. For more information, visit www.oncotelic.com.

Source Statement

This curated news summary relied on content disributed by InvestorBrandNetwork (IBN). Read the original source here, Oncotelic’s Deciparticle Platform Validated for IV Drug Delivery

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