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Trial · NCT04589845

Tumor-agnostic Precision Immuno-oncology and Somatic Targeting Rational for You (TAPISTRY) Platform Study

NCT04589845, Phase 2, Active not recruiting, Hoffmann-La Roche

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Tumor-agnostic Precision Immuno-oncology and Somatic Targeting Rational for You (TAPISTRY) Platform Study. Trials, record NCT04589845. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04589845

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Tumor-agnostic Precision Immuno-oncology and Somatic Targeting Rational for You (TAPISTRY) Platform Study
NCT number
NCT04589845
Status
Active not recruiting
Phases
Phase 2
Enrollment
920 participants, estimated
Lead sponsor
Hoffmann-La Roche
Conditions
Solid Tumors
Interventions
Entrectinib, Entrectinib, Alectinib, Atezolizumab, Ipatasertib, Trastuzumab emtansine, Inavolisib, Belvarafenib, Pralsetinib, Divarasib, Camonsertib
First posted
2020-10-19
Last updated
2026-09-04
Other registries' IDs
eudract:2020-001847-16

Source ClinicalTrials.gov

Registered outcomes41

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primary
All Cohorts: Independent Review Committee (IRC)-assessed Objective Response Rate (ORR) Based on Confirmed Objective Response (OR) per Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST v1.1)
Approximately up to 12 yearsConfirmed objective response indicates ≥4 weeks after initial documentation of response.
SecondaryAll Cohorts: IRC-assessed Duration of Response (DOR) per RECIST v1.1Approximately up to 12 years
SecondaryAll Cohorts: IRC-assessed Clinical Benefit Rate (CBR) per RECIST v1.1Approximately up to 12 years
SecondaryAll Cohorts: IRC-assessed Progression-free Survival (PFS) per RECIST v1.1Approximately up to 12 years
SecondaryAll Cohorts: Investigator (INV)-assessed ORR per RECIST v1.1Approximately up to 12 years
SecondaryAll Cohorts: INV-assessed DOR per RECIST v1.1Approximately up to 12 years
SecondaryAll Cohorts: INV-assessed CBR per RECIST v1.1Approximately up to 12 years
SecondaryAll Cohorts: INV-assessed PFS per RECIST v1.1Approximately up to 12 years
SecondaryAll Cohorts: IRC- and INV-assessed Time to Central Nervous System (CNS) Progression per RECIST v1.1Approximately up to 12 years
SecondaryAll Cohorts: Overall Survival (OS)Approximately up to 12 years

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
40086048DERIVEDPubMed
41213248DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04589845

GET https://conductscience.org/api/trials/v1/NCT04589845/registered?page=2