Submit Modified Informed Consent Form with details: CDSCO Panel Tells Sanofi om Multiple Sclerosis Drug Tolebrutinib
Written By : Dr. Divya Colin
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2024-01-21 12:30 GMT | Update On 2024-03-22 16:33 GMT
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New Delhi: Reviewing the Phase III clinical study protocol of Tolebrutinib presented by the drug major Sanofi, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has recommended the firm submit the modified Informed Consent Form mentioning the details about 11 times visit to the site.
Furthermore, the expert panel suggested the firm to submit the volume of samples to be collected and compensation to be paid in case of a visit to the site or home visit, clearance for shipping of samples outside the country, if any, and written assurance for a home visit if the patient is unable to visit the site.
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