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ZLAB biotech catalysts & pipeline

ZAI LAB LTD · Data as of 2026-09-08

Upcoming catalysts

Efgartigimod (FcRn) — Topline data

H2 2026

Thyroid eye disease (TED): Zai Lab partner argenx to provide topline results from two registrational UplighTED studies in the second half of 2026.
Source filing

ZL-1503 (IL-13/IL-31R) — Initial data

H2 2026

• Report initial first-in-human data from the SAD portion of the global Phase 1/1b study in healthy volunteers, including pharmacokinetics (PK), half-life, pharmacodynamic biomarkers (including pSTAT6), and safety, in the second half of 2026.
Source filing

ZL-1311 — IND submission

Late 2026

• Submit an IND application in the U.S. by year-end 2026 and initiate a global Phase 1 study in the first half of 2027.
Source filing

Povetacicept (APRIL/BAFF) — PDUFA

Nov 30

In June 2026, Zai Lab partner Vertex announced that the FDA accepted its BLA submission for pove for accelerated approval in adults with immunoglobulin A nephropathy (IgAN), with a PDUFA target action date of November 30, 2026.
Source filing

Elegrobart — Topline data

2027

• Zai Lab to provide topline results from the China Phase 3 registrational study in 2027.
Source filing

ZL-1222 (PD-1 / IL-12) — IND submission

2027

• Submit an IND application in the U.S. and initiate a global Phase 1 study in 2027.
Source filing

ZL-1503 (IL-13/IL-31R) — Initial data

H1 2027

• Continue enrollment in the MAD portion of the Phase 1/1b study in patients with atopic dermatitis. Initial clinical data from the MAD portion expected in the first half of 2027.
Source filing

ZL-6201 — Topline data

H1 2027

• Provide topline results from the dose escalation portion of the global Phase 1a/b study evaluating ZL-6201 in patients with sarcoma and selected tumors in the first half of 2027.
Source filing

zocilurtatug pelitecan — Conference presentation

Oct 23–Oct 27

Global Phase 1 data for zocilurtatug pelitecan (zoci) in combination with a PD-L1 inhibitor in first-line SCLC to be presented at ESMO 2026; planned initiation of a registrational Phase 3 study later this year
Source filing

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