PPI Pharmaceuticals

About us

A South Carolina oncology company built on academic discovery

PPI Pharmaceuticals, LLC was founded in South Carolina in November 2013 as a spin-off from an academic research laboratory. Campbell McInnes, Ph.D., Professor in Medicinal Chemistry at the University of South Carolina, is President and Chief Scientific Officer. The company develops next-generation cancer therapeutics by using novel technology to exploit protein-protein interactions.

Key accomplishments

  1. November 2013

    PPI Pharmaceuticals, LLC founded in South Carolina

  2. May 2017 – May 2021

    Polo-box PLK1 Inhibitors Target Tumors Resistant to ATP Competitive Compounds (Phase I STTR).

    Full in vivo validation of the REPLACE strategy in prostate cancer

  3. Aug 2025 – present

    Polo-box PLK1 Inhibitors Target Tumors Resistant to ATP Competitive Compounds (Phase I STTR).

    Further in vivo validation in colorectal cancer using patient derived tumors. Striving towards personalized cancer treatment.

  4. September 2026

    Phase II grant applied for ($2.5 M over 2 years).

    Involves determining in vivo activity in a colon cancer model.

Business model

Out-license partnered development

The business model of most small companies is to out-license to larger pharmaceutical companies. For partnered drug development, sales are handled by the major company that has in-licensed PPI technology.

Founded
November 2013, South Carolina
Industry
Pharmaceutical / biotechnology research and development

Route to Market

Around 100 projects narrow to 10 compounds, then to 1 drug. Funding shifts from grants to investors, then to a pharmaceutical partner.

Development pathDiscovery, development, and delivery. Around 100 projects, 10 compounds, and 1 drug, funded by academic grants, STTR and SBIR awards, investors, and an out-license to a pharmaceutical partner.1. DISCOVERY2. DEVELOPMENT3. DELIVERYIDEABASIC RESEARCHThe majority of theresearch at thisstage is publiclyfunded at universities,colleges andindependent researchinstitutionsin every state.100 projectsCLINICAL TRIALSOnce a disease target is identified,drugs are designed and tested.Both public and privately fundedresearch are involved.10 compoundsPHASE IPHASE IIPHASE IIIREGULATORY APPROVALHuman trials are completed. FDAapproval. Industry is responsiblefor bringing a drug to market. Safetyand evaluation continue after approvals.1 drugPATIENT CAREACADEMIC GRANTS$150,000PHASE I AND IISTTR / SBIR$2 millionINVESTORS$4 million / trialOUT-LICENSE TO A PHARMA PARTNERPhase II · $10–15 millionPhase III · $20–30 million