Extended indication Soquelitinib monotherapy for third line or later treatment of relapsed or refractory peripheral T-cell lymphoma in adults and elderly.
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Soquelitinib
Domain Hematology
Reason of inclusion New medicine (specialité)
Main indication Aggressive non-Hodgkin’s lymphoma
Extended indication Soquelitinib monotherapy for third line or later treatment of relapsed or refractory peripheral T-cell lymphoma in adults and elderly.
Manufacturer Corvus
Portfolio holder Corvus
Route of administration Oral
Therapeutical formulation Capsule
Budgetting framework Intermural (MSZ)

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
ATMP No
Submission date May 2026
Expected Registration June 2027
Orphan drug Yes
Registration phase Clinical trials

Therapeutic value

Therapeutic value No estimate possible yet

This assessment does not indicate any potential inclusion in the package.

References NCT06561048

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

References Zhang & Dalal. Value in Health. 2019 (1).
Additional remarks Perifeer T-cellymfoom is een zeldzame aandoening. De incidentie voor perifeer T-cellymfoom wordt geschat op 0,62 per 100.000 (1), wat neerkomt op zo'n 110 diagnoses in Nederland per jaar.

Expected cost per patient per year

Potential total cost per year

Off label use

Indication extension

Other information