Pharming Group provides updates on EMA regulatory review of leniolisib MAA and plans to file for UK regulatory approval - Seite 3

Inside Information

This press release relates to the disclosure of information that qualifies, or may have qualified, as inside information within the meaning of Article 7(1) of the EU Market Abuse Regulation.

References

1. Lucas CL, et al. Nat Immunol. 2014;15(1):88-97.
2. Elkaim E, et al. J Allergy Clin Immunol. 2016;138(1):210-218.  
3. Nunes-Santos C, Uzel G, Rosenzweig SD. J Allergy Clin Immunol. 2019;143(5):1676-1687.  
4. Coulter TI, et al. J Allergy Clin Immunol. 2017;139(2):597-606.  
5. Maccari ME, et al. Front Immunol. 2018;9:543.  
6. Jamee M, et al. Clin Rev Allergy Immunol. 2019;May 21.  
7. Condliffe AM, Chandra A. Front Immunol. 2018;9:338.
8. RAO VK, et al Blood. 2023 Mar 2;141(9):971-983

For further public information, contact:

Pharming Group, Leiden, The Netherlands
Michael Levitan, VP Investor Relations & Corporate Communications
T: [phone]

Heather Robertson, Investor Relations & Corporate Communications Manager
E: [e-mail]

FTI Consulting, London, UK
Victoria Foster Mitchell/Alex Shaw/Amy Byrne
T: [phone]

LifeSpring Life Sciences Communication, Amsterdam, The Netherlands
Leon Melens
T: [phone]
E: [e-mail]

US PR
Ethan Metelenis
E: [e-mail]
T: [phone]