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A Data Collection Study for Patients With Adenocarcinoma Treated With the MyVaccx Immunotherapy Regimen.

A Retrospective and Prospective Study of a New Immunotherapy Regimen (MyVaccx) for Patients With Adenocarcinoma.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03695835
Acronym
NIRPA
Enrollment
27
Registered
2018-10-04
Start date
2018-04-11
Completion date
2020-06-17
Last updated
2020-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adenocarcinoma

Keywords

prostate cancer, lung cancer, pancreatic cancer, colorectal cancer, bladder cancer

Brief summary

A retrospective and prospective data collection study on 27 consecutive subjects with adenocarcinoma who were treated using the MyVaccx system by Dr. Gary Onik. Retrospective data were collected on the treatment with the immunotherapy system and prospective data will be collected as they are prospectively monitored through their normal standard of care for their original cancer.

Interventions

DRUGImmunotherapeutic Agents

Antigen exposure immediately followed by in situ injection of combination of immunotherapeutic agents

DEVICEAblation

Antigen exposure immediately followed by in situ injection of combination of immunotherapeutic agents

Sponsors

Gary Onik MD
Lead SponsorINDIV

Study design

Observational model
CASE_ONLY
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Treatment with the MyVaccx System * Greater than 18 years of age * Signature of the informed consent

Exclusion criteria

* 2 subjects treated with the MyVaccx System with known visceral disease

Design outcomes

Primary

MeasureTime frameDescription
MyVaccx immunotherapy treatment impact on late stage cancer diseaseFrom date of treatment until the date of death from any cause up to 60 monthsTime to death after the start of treatment

Secondary

MeasureTime frameDescription
MyVaccx immunotherapy treatment impact on late stage cancer diseaseTime to progression after a complete or partial response up to 60 monthsComplete and partial response to treatment based on the iRESIST criteria

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026