fgfr inhibitor clinical trial assay (cta) Search Results


90
Janssen fgfr inhibitor clinical trial assay (cta)
Study design and sample selection. *Includes 1 untreated patient in regimen 3. ** n = 600 samples were not eligible for the bridging study (reasons: received before November 28, 2015, no consent for bridging testing, insufficient samples or passing sample store limit). † Includes 1 <t>FGFR+</t> patient who was not treated but was eligible for the bridging study. ‡ 320 patients were randomly selected and then 120 patients were removed due to a change in the selecting protocol. CDx, companion diagnostic assay; <t>CTA,</t> clinical trial assay; FGFR, fibroblast growth factor receptor; ORR, objective response rate.
Fgfr Inhibitor Clinical Trial Assay (Cta), supplied by Janssen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fgfr inhibitor clinical trial assay (cta)/product/Janssen
Average 90 stars, based on 1 article reviews
fgfr inhibitor clinical trial assay (cta) - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

90
Almac Inc fgfr inhibitor clinical trial assay (cta)
Study design and sample selection. *Includes 1 untreated patient in regimen 3. ** n = 600 samples were not eligible for the bridging study (reasons: received before November 28, 2015, no consent for bridging testing, insufficient samples or passing sample store limit). † Includes 1 <t>FGFR+</t> patient who was not treated but was eligible for the bridging study. ‡ 320 patients were randomly selected and then 120 patients were removed due to a change in the selecting protocol. CDx, companion diagnostic assay; <t>CTA,</t> clinical trial assay; FGFR, fibroblast growth factor receptor; ORR, objective response rate.
Fgfr Inhibitor Clinical Trial Assay (Cta), supplied by Almac Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fgfr inhibitor clinical trial assay (cta)/product/Almac Inc
Average 90 stars, based on 1 article reviews
fgfr inhibitor clinical trial assay (cta) - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

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Study design and sample selection. *Includes 1 untreated patient in regimen 3. ** n = 600 samples were not eligible for the bridging study (reasons: received before November 28, 2015, no consent for bridging testing, insufficient samples or passing sample store limit). † Includes 1 FGFR+ patient who was not treated but was eligible for the bridging study. ‡ 320 patients were randomly selected and then 120 patients were removed due to a change in the selecting protocol. CDx, companion diagnostic assay; CTA, clinical trial assay; FGFR, fibroblast growth factor receptor; ORR, objective response rate.

Journal: The Journal of Pathology: Clinical Research

Article Title: Identifying fibroblast growth factor receptor genetic alterations using RNA‐based assays in patients with metastatic or locally advanced, surgically unresectable, urothelial carcinoma who may benefit from erdafitinib treatment

doi: 10.1002/cjp2.163

Figure Lengend Snippet: Study design and sample selection. *Includes 1 untreated patient in regimen 3. ** n = 600 samples were not eligible for the bridging study (reasons: received before November 28, 2015, no consent for bridging testing, insufficient samples or passing sample store limit). † Includes 1 FGFR+ patient who was not treated but was eligible for the bridging study. ‡ 320 patients were randomly selected and then 120 patients were removed due to a change in the selecting protocol. CDx, companion diagnostic assay; CTA, clinical trial assay; FGFR, fibroblast growth factor receptor; ORR, objective response rate.

Article Snippet: The FGFR inhibitor Clinical Trial Assay (CTA), a RT‐PCR assay developed by Janssen, USA, and performed by Almac Diagnostics (Craigavon, UK) was used to determine the FGFR alteration status in patients enrolled for the erdafitinib phase 2 study.

Techniques: Selection, Diagnostic Assay

Concordance analysis for CDx and  CTA  (reference)  FGFR  gene mutation screening methods

Journal: The Journal of Pathology: Clinical Research

Article Title: Identifying fibroblast growth factor receptor genetic alterations using RNA‐based assays in patients with metastatic or locally advanced, surgically unresectable, urothelial carcinoma who may benefit from erdafitinib treatment

doi: 10.1002/cjp2.163

Figure Lengend Snippet: Concordance analysis for CDx and CTA (reference) FGFR gene mutation screening methods

Article Snippet: The FGFR inhibitor Clinical Trial Assay (CTA), a RT‐PCR assay developed by Janssen, USA, and performed by Almac Diagnostics (Craigavon, UK) was used to determine the FGFR alteration status in patients enrolled for the erdafitinib phase 2 study.

Techniques: Mutagenesis

Investigator‐assessed ORR in erdafitinib‐treated patients who were  FGFR+  by both CDx and  CTA  assays

Journal: The Journal of Pathology: Clinical Research

Article Title: Identifying fibroblast growth factor receptor genetic alterations using RNA‐based assays in patients with metastatic or locally advanced, surgically unresectable, urothelial carcinoma who may benefit from erdafitinib treatment

doi: 10.1002/cjp2.163

Figure Lengend Snippet: Investigator‐assessed ORR in erdafitinib‐treated patients who were FGFR+ by both CDx and CTA assays

Article Snippet: The FGFR inhibitor Clinical Trial Assay (CTA), a RT‐PCR assay developed by Janssen, USA, and performed by Almac Diagnostics (Craigavon, UK) was used to determine the FGFR alteration status in patients enrolled for the erdafitinib phase 2 study.

Techniques:

Study design and sample selection. *Includes 1 untreated patient in regimen 3. ** n = 600 samples were not eligible for the bridging study (reasons: received before November 28, 2015, no consent for bridging testing, insufficient samples or passing sample store limit). † Includes 1 FGFR+ patient who was not treated but was eligible for the bridging study. ‡ 320 patients were randomly selected and then 120 patients were removed due to a change in the selecting protocol. CDx, companion diagnostic assay; CTA, clinical trial assay; FGFR, fibroblast growth factor receptor; ORR, objective response rate.

Journal: The Journal of Pathology: Clinical Research

Article Title: Identifying fibroblast growth factor receptor genetic alterations using RNA‐based assays in patients with metastatic or locally advanced, surgically unresectable, urothelial carcinoma who may benefit from erdafitinib treatment

doi: 10.1002/cjp2.163

Figure Lengend Snippet: Study design and sample selection. *Includes 1 untreated patient in regimen 3. ** n = 600 samples were not eligible for the bridging study (reasons: received before November 28, 2015, no consent for bridging testing, insufficient samples or passing sample store limit). † Includes 1 FGFR+ patient who was not treated but was eligible for the bridging study. ‡ 320 patients were randomly selected and then 120 patients were removed due to a change in the selecting protocol. CDx, companion diagnostic assay; CTA, clinical trial assay; FGFR, fibroblast growth factor receptor; ORR, objective response rate.

Article Snippet: The FGFR inhibitor Clinical Trial Assay (CTA), a RT‐PCR assay developed by Janssen, USA, and performed by Almac Diagnostics (Craigavon, UK) was used to determine the FGFR alteration status in patients enrolled for the erdafitinib phase 2 study.

Techniques: Selection, Diagnostic Assay

Concordance analysis for CDx and  CTA  (reference)  FGFR  gene mutation screening methods

Journal: The Journal of Pathology: Clinical Research

Article Title: Identifying fibroblast growth factor receptor genetic alterations using RNA‐based assays in patients with metastatic or locally advanced, surgically unresectable, urothelial carcinoma who may benefit from erdafitinib treatment

doi: 10.1002/cjp2.163

Figure Lengend Snippet: Concordance analysis for CDx and CTA (reference) FGFR gene mutation screening methods

Article Snippet: The FGFR inhibitor Clinical Trial Assay (CTA), a RT‐PCR assay developed by Janssen, USA, and performed by Almac Diagnostics (Craigavon, UK) was used to determine the FGFR alteration status in patients enrolled for the erdafitinib phase 2 study.

Techniques: Mutagenesis

Investigator‐assessed ORR in erdafitinib‐treated patients who were  FGFR+  by both CDx and  CTA  assays

Journal: The Journal of Pathology: Clinical Research

Article Title: Identifying fibroblast growth factor receptor genetic alterations using RNA‐based assays in patients with metastatic or locally advanced, surgically unresectable, urothelial carcinoma who may benefit from erdafitinib treatment

doi: 10.1002/cjp2.163

Figure Lengend Snippet: Investigator‐assessed ORR in erdafitinib‐treated patients who were FGFR+ by both CDx and CTA assays

Article Snippet: The FGFR inhibitor Clinical Trial Assay (CTA), a RT‐PCR assay developed by Janssen, USA, and performed by Almac Diagnostics (Craigavon, UK) was used to determine the FGFR alteration status in patients enrolled for the erdafitinib phase 2 study.

Techniques: