Ad hoc announcement pursuant to Art. 53 LR
Management call today at 3.30 pm CEST
Newron received the anticipated FDA written communication on clinical hold at U.S. study centers
Ad hoc announcement pursuant to Art. 53 LR
U.S. clinical hold remains in place; study continues in all other countries
Company initiates expansion of clinical sites and enrollment
Ad hoc announcement pursuant to Art. 53 LR
Milan, Italy, and Morristown, NJ, USA – September 22, 2026, 07:00 am CET – Newron Pharmaceuticals S.p.A. (“Newron”) (SIX: NWRN, XETRA:
Ad hoc announcement pursuant to Art. 53 LR
Total proceeds expected to fund global ENIGMA-TRS studies and extend cash runway beyond pivotal 12-week results, supporting development
Milan, Italy, and Morristown, NJ, USA, September 3, 2026, – Newron Pharmaceuticals S.p.A. (“Newron”) (SIX: NWRN, XETRA: NP5), a biopharmaceutical company focused on the
Ad hoc announcement pursuant to Art. 53 LR
ENIGMA-TRS 1 is Phase 3 international, one-year, randomized, double-blind, placebo-controlled study in 600+ patients; 12-week study
Ad hoc announcement pursuant to Art. 53 LR
Parties discussed information provided by Newron and changes needed by FDA to consider re-start of enrollment in ENIGMA-TRS 2 study in
Milan, Italy, and Morristown, NJ, USA – May 28, 2026, 3:30 pm CEST – Newron Pharmaceuticals S.p.A. (“Newron”) (SIX: NWRN, XETRA: NP5), a biopharmaceutical company focused on the
Ad hoc announcement pursuant to Art. 53 LR
Newron reports a pause in enrollment of new study participants in US centers of ENIGMA-TRS 2 study
Pause of enrollment limited to US
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