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This medicinal product has been authorised under a 'conditional approval' scheme. This means that further evidence on this medicinal product is awaited.

Real-world effectiveness of ZYNLONTA monotherapy in patients with R/R DLBCL following CAR-T therapy1

RWE Study design
Best response for Zynlonta 3L 4L
ZYNLONTA in CAR-T therapy respondent patients compared to refractory patients
ZYNLONTA in CAR-T therapy respondent patients compared to refractory patients
ZYNLONTA treatment characteristics and discontinuations
ZYNLONTA treatment characteristics and discontinuations

This medicine is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to Swedish Orphan Biovitrum Ltd by email at [email protected] or by calling +44 (0) 800 111 4754.

Abbreviations:
2L / 3L / 4L: second line, third line, fourth line; AEs: adverse events; ALT: alanine aminotransferase; AST: aspartate aminotransferase; CAR-T: chimeric antigen receptor T-cell; CR: complete response; DOR: duration of response; IQR: interquartile range; ORR: overall response rate; OS: overall survival; PR: partial response; PFS: progression-free survival; ULN: upper limit of normal

References:
1. Epperla N et al. Blood Cancer Journal 2024; 14: 210. 2. Epperla N et al. Blood Cancer Journal 2024; 14: 210. (Suppl.)

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