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NEXTAR - NEXavar® as First TARgeted Treatment for Patients With Advanced Renal Cell Carcinoma


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N/A
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Open (Enrolling)
Both
Carcinoma, Renal Cell

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Trial Information

NEXTAR - NEXavar® as First TARgeted Treatment for Patients With Advanced Renal Cell Carcinoma


Inclusion Criteria:



- Patients with a diagnosis of advanced Renal cell carcinoma (RCC) for whom the
decision has been taken by the investigator to prescribe Nexavar.

- Patients who failed cytokine therapy or who are not suitable for cytokines for whom
Nexavar is the first targeted drug treatment.

Exclusion Criteria:

- Prior targeted therapy for RCC

- Contraindications of Nexavar described in the Summary of Product Characteristics
(SPC).

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

Duration of Nexavar treatment

Outcome Time Frame:

up to 3 years

Safety Issue:

No

Principal Investigator

Bayer Study Director

Investigator Role:

Study Director

Investigator Affiliation:

Bayer

Authority:

Germany: Federal Institute for Drugs and Medical Devices

Study ID:

16091

NCT ID:

NCT01508364

Start Date:

July 2012

Completion Date:

March 2015

Related Keywords:

  • Carcinoma, Renal Cell
  • renal cell carcinoma, first targeted therapy, observational study
  • Carcinoma
  • Carcinoma, Renal Cell

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