Recruiting

Precision Oncology

Sponsor:

SpeciCare

Code:

NCT03896958

Conditions

Cancer, All Types

Cancer of Liver

Cancer of Stomach

Cancer of Head and Neck

Cancer of Rectum

Eligibility Criteria

Sex: All

Age: 0 - 70+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

The PIONEER Initiative stands for Precision Insights On N-of-1 Ex vivo Effectiveness Research. The PIONEER Initiative is designed to provide access to functional precision medicine to any cancer patient with any tumor at any medical facility. Tumor tissue is saved at time of biopsy or surgery in multiple formats, including fresh and cryopreserved as a living biospecimen. SpeciCare assists with access to clinical records in order to provide information back to the patient and the patient's clinical care team. The biospecimen tumor tissue is stored in a bio-storage facility and can be shipped anywhere the patient and the clinical team require for further testing. Additionally, the cryopreservation of the biospecimen allows for decisions about testing to be made at a later date. It also facilitates participation in clinical trials. The ability to return research information from this repository back to the patient is the primary end point of the study. The secondary end point is the subjective assessment by the patient and his or her physician as to the potential benefit that this additional information provides over standard of care. Overall the goal of PIONEER is to enable best in class functional precision testing of a patient's tumor tissue to help guide optimal therapy (to date this type of analysis includes organoid drug screening approaches in addition to traditional genomic profiling).

Conditions

Cancer, All Types

Cancer of Liver

Cancer of Stomach

Cancer of Head and Neck

Cancer of Rectum

Study ID

NCT03896958

Start date

Mar 21, 2019

Status verified date

Dec, 2020

Completion date

Mar 12, 2024

Anticipated

Primary completion date

Mar 12, 2024

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

- All patients diagnosed with cancer and all patients at risk of cancer

Exclusion Criteria:

-Patients who decline definitive therapies Patients with comorbidities that prevent definitive therapies Patients on hospice

Study Design

Enrollment

1000 participants

Anticipated

Interventions and Outcome Measures

Primary outcome measure

  • Return of research information [ Time Frame: Two Years ]
  • Assessment of benefit of return of research results [ Time Frame: Two Years ]
  • Assessment of benefit of return of research results by SpeciCare Outcome Monitor Board [ Time Frame: Two Years ]

Central Contacts and Locations

Central contacts

Locations

Specicare

Recruiting

Gainesville, Georgia, United States, 30501

Contacts

More Information

Sponsor

SpeciCare

Last update posted

Dec 4, 2020

Last verified

Dec, 2020

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by SpeciCare on 2020-12-04.