ReportGem ReportGem 中文

GLOBAL RESEARCH ARCHIVE

MLTX - 1Q26; Positive Pre-BLA Meeting Outcome Aligns With Best-Case Outcome for Competitive Labeling in HS; VELA-TEEN to Expand Label Further; PsA Readouts Remain On-Track

Published: 2026-05-11Institution: Guggenheim Securities LLCCompany / ticker: MLTX.OQPages: 7Original language: 英语Evidence page: 1

Research evidence excerpt

MLTX - 1Q26; Positive Pre-BLA Meeting Outcome Aligns With Best-Case Outcome for Competitive Labeling in HS; VELA-TEEN to Expand Label Further; PsA Readouts Remain On-Track

May 11, 2026

Yatin Suneja yatin.suneja@guggenheimpartners.com MLTX - 1Q26; Positive Pre-BLA Meeting Outcome

212 518 9565 Aligns With Best-Case Outcome for Competitive

Min Lee, Ph.D.

min.lee@guggenheimpartners.com Labeling in HS; VELA-TEEN to Expand Label Further;

212 823 6744 PsA Readouts Remain On-Track Iris Gao, Ph.D.

iris.gao@guggenheimpartners.com

212 518 9013 Key Message: Yesterday, MLTX reported 1Q26 earnings and provided key new

Eddie Hickman, Ph.D. corporate updates: (1) HS & BLA updates: On Apr 1st, MLTX held a pre-BLA meeting

eddie.hickman@guggenheimpartners.com with the FDA. As expected, the FDA confirmed acceptability of MIRA trial to establish

212 518 9904 substantial evidence of effectiveness (SEE), as well as inclusion of VELA-TEEN

Delma Caiati, M.D., Ph.D. data for the final label that covers adolescent HS patients ages 12 & above (see note

delma.caiati@guggenheimpartners.com HERE; broadest HS label to-date). Per mgmt, these adolescent HS patients represent

617 859 4606 ~10% of the total HS market, effectively enabling sonelokimab (SLK; dual IL-17A/

F targeting nanobody) to capture a broader HS population that is not included in

UCB's Bimzelx's label. These outcomes support the company's upside case, potentially

including a blended HiSCR-75 of pbo-adj. ~Δ23% (Recall that VELA-1 & MIRA showed

MLTX BUY ~Δ17%option. BLA& ~Δ29%,submissionrespectively),is expectedwhichforcouldend supportof Sept, sonelokimabwith potentialasBLAa BICacceptancetreatment

MoonLake Immunotherapeutics as early as end of Nov 2026 (contingent upon decision of Priority Review designation,

The English excerpt is extracted automatically from the cited source page and may contain layout or recognition errors. It is never batch translated.

Open report viewer