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MCW Master Predict (Profile Related Evidence Determining Individualized Cancer Therapy)

Medical College of Wisconsin Master Predict (Profile Related Evidence Determining Individualized Cancer)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05802069
Enrollment
10000
Registered
2023-04-06
Start date
2022-12-19
Completion date
2027-12-31
Last updated
2025-08-17

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

Conditions

Cancer

Brief summary

The study is an observational trial for patients undergoing cancer-related interventions and therapy at Medical College of Wisconsin Cancer Center. Projects under this protocol will use patient data that will be collected both retrospectively and prospectively. It will also enable prospective sample collection for specific cancer-related studies.

Detailed description

This is a master protocol that enables investigators to conduct observational research and correlative biospecimen studies. This study is non-therapeutic, with retrospective and prospective components. This will be a single-site study at MCW/FH. Retrospective data and, with consent, prospective observational data will be collected. The study will also include an opportunity for patients to consent to the analysis of specimens collected prospectively during care and for the collection of research-related testing of blood, stool, and/or urine. It is designed to decrease the burden on both patients and investigators by allowing consent to a protocol that will enable multiple minimal-risk studies. Studies under this master protocol may perform data analysis using standard statistical techniques, as well as with advanced bioinformatics, machine learning, artificial intelligence, and other related technologies. Collection and testing of biospecimens will only be performed if a proposed study that falls under this master protocol requires it. Studies may include a variety of simple or advanced techniques related to chemical, hematologic, molecular, proteomic, transcriptomic, immunomic, and metabolic analyses, as well as related multi-omic analysis for biomarker discovery, understanding correlations between treatment and molecular features, and/or for pharmacokinetic (PK) and pharmacodynamic (PD) parameters.

Interventions

None listed

Sponsors

Sameem M. Abedin, MD
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

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

Inclusion criteria

* Subjects aged 18 years and older who were previously or are currently receiving care for a cancer-related condition at MCW/FH.

Design outcomes

Primary

MeasureTime frameDescription
Number of subjects receiving precision therapies providing biospecimens of any kind.One yearPrecision therapies are targeted against specific genomic mutations.
Number of subjects not receiving precision therapies and providing biospecimens.One yearPrecision therapies are targeted against specific genomic mutations.

Countries

United States

Contacts

Primary ContactKristina Jacobs
kjacobs@mcw.edu414-955-3643
Backup ContactMedical College of Wisconsin Cancer Center Clinical Trials Office
cccto@mcw.edu866-680-0505

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 30, 2026