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Prospective, Multicentric, Large Scale Observational Study to Evaluate Effectiveness and Safety of Nexavar® in Advanced Renal Cell Carcinoma


Phase 4
N/A
N/A
Not Enrolling
Both
Carcinoma, Renal Cell

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Trial Information

Prospective, Multicentric, Large Scale Observational Study to Evaluate Effectiveness and Safety of Nexavar® in Advanced Renal Cell Carcinoma


Inclusion Criteria:



- Patients with diagnosis of advanced Renal Cell Carcinoma (RCC) and decision taken by
the investigator to prescribe Sorafenib

Exclusion Criteria:

- Exclusion criteria must be read in conjunction with the local product information.

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

Efficacy related variables are status of tumor / metastases.

Outcome Time Frame:

After 12 months, or at discontinuation of therapy or at end of study (whatever is earlier)

Safety Issue:

No

Principal Investigator

Bayer Study Director

Investigator Role:

Study Director

Investigator Affiliation:

Bayer

Authority:

India: Drugs Controller General of India

Study ID:

15246

NCT ID:

NCT01353794

Start Date:

March 2013

Completion Date:

January 2016

Related Keywords:

  • Carcinoma, Renal Cell
  • SORAFENIB
  • RENAL CELL CARCINOMA
  • TYROSINE KINASE INHIBITOR
  • OBSERVATIONAL STUDY
  • Carcinoma
  • Carcinoma, Renal Cell

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