To determine the safety of sirolimus tablets in renal allograft recipients in a postmarketing surveillance setting.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Unnamed facility
Bangalore, Karnataka, India
Unnamed facility
Bangalore, Karnataka, India
Unnamed facility
Sāket, South Delhi, India
Unnamed facility
Chennai, Tamil Nadu, India
Unnamed facility
New Delhi, India
Safety evaluation
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