Our mission

We strive to develop innovative therapeutics, to eliminate cancers, and prevent recurrence.
We aim to provide better and more accessible treatment options to diverse patient populations around the world.
We fight every day because we know patients do too.

Confront Challenging Conditions

Adaptive therapeutics for multiple indications.

Maximize Benefit of Local and Regional Delivery

Increased efficacy through targeted treatment.

Patients First

Drug design inspired by the patient experience

Streamlined Solution-Focused Research and Development

Honing imaginative thinking into accessible products
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PRV Platform Technology

Transforming innovation to hope through action.

The PRV™ platform enables targeted therapy while avoiding systemic toxicity to provide a safer, less invasive alternative to currently available treatments
The PRV™ system is available in multiple dosage forms. Formulations include topical and intraoperatively administered patches, hydrogels and intratumoral injectables.

The lead indication for PRV111 is head and neck cancer. Other indications for PRV products are:

  • Carcinoma in situ
  • Lung Cancer
  • Colorectal Cancer
  • Penile Cancer
  • Esophagus Cancer
  • Cervical/Vaginal/Vulvar Cancer
  • Anal Cancer
  • Ocular Squamous Cell Carcinoma

The PRV system is currently used for locoregional treatment of cancerous tumors and precancerous lesions of the oral cavity. Additional formulations and treatment strategies comprising compounds for other cancers and indications outside of oncology are under development, with promising results.

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Pipeline

The lead indication of the PRV System is oral cancer, followed by oral carcinoma in situ and intra-operative chemotherapy cancers. Privo’s Phase II clinical study on oral cancer has successfully completed meeting all of its primary and secondary endpoints. Privo oral carcinoma in situ is in phase 3

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Recognition

Privo is excited to work closely with its collaborators at the FDA, the NCI and the NIDCR.
Privo Technologies has received over $20M in nondilutive funding from these institutions in support of its product development and clinical trial.

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