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Expanded Access for PSV Personalized Oncolytic Viruses

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EpicentRx

Status

Conditions

Cancer

Treatments

Drug: PSV

Study type

Expanded Access

Funder types

Industry

Identifiers

Details and patient eligibility

About

A compassionate use, expanded access protocol for patients who have exhausted all standard therapy having progressed on chemotherapy and immunotherapy.

Full description

Patients will receive intratumoral or subcutaneous injection of an oncolytic virus called PSV (short for Personalized Virus) every other week until the occurrence of immune related RECIST progression, intolerable toxicity, change to another anti-cancer treatment due to lack of apparent benefit, or personal choice.

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Ability to understand and sign a written informed consent form.

  • Measurable or evaluable disease with least one (1) tumor that is accessible to intratumoral injection.

  • Eastern Cooperative Group (ECOG) performance status is 0-3 at Screening.

  • Acceptable liver function at Screening, as evidenced by:

    • Bilirubin ≤ 3.0 X upper limit of normal (ULN) since this patient has
    • been diagnosed with Gilbert's Disease
  • AST (SGOT) and ALT (SGPT) ≤ 5 X ULN.

  • Serum creatinine < 3 x institution upper limit of normal.

  • Patient has acceptable hematologic status at Screening, as evidenced by:

    • Absolute neutrophil count ≥ 1,500 cells/mm3; and
    • Platelet count ≥ 70,000/mm3; and
    • Hemoglobin (HGB) ≥ 8.5 g/dL.
  • Medically acceptable contraception.

  • Willingness to comply with all protocol procedures, evaluations and rescue measures.

Exclusion criteria

  • Presence of a serious co-morbid medical condition, or a clinically significant laboratory finding(s) that, in the opinion of the Investigator, suggests the presence of an infectious, endocrine, and/or other inadequately treated systemic disorder.
  • An active bacterial, fungal, or viral infection.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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