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pPJV7630

phase 1 PowderMed

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DeveloperPowderMed
PlatformDNA
HSV targetHSV-2
Approachtherapeutic
Phasephase 1
StatusTwo Phase 1 trials were completed by 2006 with no results posted on the registry; as of the 2026-09-27 registry search, no record naming pPJV7630 has an ongoing status.
Trials NCT00274300 , NCT00310271

pPJV7630 is a DNA vaccine for HSV-2 that its PowderMed-sponsored registry record describes as therapeutic. It was studied in a phase 1 dose-escalating trial in people with recurrent genital herpes caused by HSV-2, completed in 2005, and in a phase 1 safety trial with pPJV2012 in HSV-2 seronegative healthy volunteers, completed in 2006. Neither trial has results posted on the registry, and as of the 2026-09-27 registry search no record naming pPJV7630 has an ongoing status.

What it is

pPJV7630 is a DNA vaccine for HSV-2, described in its registry record as therapeutic and sponsored by PowderMed. In both registered trials it was administered by PMED; the second record describes this as particle-mediated epidermal delivery using the PowderMed ND10 system.

Where it stands

NCT00274300 was a phase 1, two-center, open-label, dose-escalating study of safety, tolerability and immunogenicity in patients with recurrent genital herpes caused by HSV-2. It is listed as completed in 2005 with an enrollment figure of 36 that the record does not mark as actual or estimated, and no results are posted. NCT00310271 was a phase 1 safety and tolerability study of pPJV7630 given with pPJV2012 in HSV-2 seronegative healthy volunteers; the trial title describes a DNA vaccine with a DNA-encoded immunostimulator. It is listed as completed in 2006 with an enrollment figure of 42 that the record does not mark as actual or estimated, and no results are posted. A ClinicalTrials.gov search on 2026-09-27 for records naming pPJV7630 returned these 2 records, and none had an ongoing status.

What this does and doesn’t mean

These were phase 1 studies focused on safety, tolerability and immune response, so their existence does not show that the vaccine reduced herpes outbreaks or prevented infection. No results from either trial are posted on the registry or reported in the sources here.

Registry snapshot

Verbatim from ClinicalTrials.gov as of Sep 28, 2026. These are the registry's administrative facts; the editorial status above is our reading of the evidence and may differ.

Safety Study of HSV2 DNA Vaccine to Treat Patients With Recurrent Genital Herpes Caused by HSV-2

Registry status
Completed
Phase
phase 1
Enrollment
36
Lead sponsor
PowderMed
Started
Aug 2004

Registry record last updated Jan 29, 2007.

A Safety Study to Assess a DNA Vaccine Administered by Particle Mediated Delivery to the Skin in Healthy Subjects

Registry status
Completed
Phase
phase 1
Enrollment
42
Lead sponsor
PowderMed
Started
Apr 2006

Registry record last updated Nov 21, 2008.

Sources

  1. ClinicalTrials.gov registry search for pPJV7630 (searched 2026-09-27) — ClinicalTrials.gov , searched 2026-09-27
  2. A Phase I, Two-Center, Open-Label, Dose-Escalating Study to Investigate the Safety, Tolerability and Immunogenicity of pPJV7630, a Therapeutic DNA Vaccine for Herpes Simplex Virus Type 2 (HSV-2), in Patients With Recurrent Genital Herpes Caused by HSV-2 (NCT00274300) — ClinicalTrials.gov , record updated 2007-01-29
  3. A Phase I Study Assessing Safety and Tolerability of a DNA Vaccine With a DNA Encoded Immunostimulator , Administered by Particle Mediated Epidermal Delivery Using the PowderMed ND10 Delivery System in HSV-2 Seronegative Healthy Volunteers (NCT00310271) — ClinicalTrials.gov , record updated 2008-11-21