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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05312307
Other study ID # STR-006-001
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date February 6, 2023
Est. completion date February 22, 2024

Study information

Verified date February 2024
Source Strata Oncology
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary goal of this study is to identify patients with RNA expression profiles consistent with eligibility requirements for therapeutic clinical trials across solid tumors. Left-over tumor tissue will be collected from eligible participants for RNA expression analysis using next-generation sequencing.


Description:

The primary goal of this study is to identify patients with RNA expression profiles consistent with eligibility requirements for therapeutic clinical trials across solid tumors. Left-over tumor tissue will be collected from eligible participants for RNA expression analysis using next-generation sequencing. A parallel study, StrataPATH™ (STR-004-001), has been developed to support therapeutic hypotheses. Participants may be consented and screened for enrollment separately into StrataPATH with an eligible matching biomarker/drug treatment cohort upon positive identification of a relevant expression signature. Treatment effectiveness of antibody drug conjugates and other targeted therapies will be evaluated in these molecularly defined cohorts.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date February 22, 2024
Est. primary completion date February 22, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Must be =18 years of age, 2. Participant must have pathologically confirmed advanced, metastatic, or recurrent solid tumor, 3. Measurable disease, 4. Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2, 5. Participant must meet at least 1 of the following: 1. Is/has not adequately responded to standard therapy, or 2. For whom no life-extending standard therapy exists, or 3. Who decline standard therapy, or 4. In the opinion of the investigator, is not a candidate for or would be unlikely to tolerate or derive significant clinical benefit from standard therapy 6. Adequate cardiac, bone marrow, organ function & laboratory parameters as determined by the treating physician for potential participation in a clinical trial, 7. Leftover formalin-fixed, paraffin-embedded (FFPE) tumor tissue available for StrataEXP testing Exclusion Criteria: 1. Females who are pregnant or nursing, 2. History of stroke including transient ischemic attack (TIA) or acute myocardial infarction within 4 months of enrollment, 3. Any other clinically significant medical condition that, in the opinion of the treating physician, makes participation in a clinical trial undesirable, including but not limited to ongoing or active infection, significant uncontrolled hypertension, or severe psychiatric illness.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Strata Oncology

Outcome

Type Measure Description Time frame Safety issue
Primary To identify subjects with RNA signatures who may be eligible for clinical trial enrollment The percentage of participants identified as eligible for therapeutic clinical trials. 5 years
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