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Zai Lab (ZLAB) pipeline and stated timing

Pipeline at a glance

ProgramEventStageStated timingFiling
ZL-1503 SAD/data readoutPhase 1in the second half of 20268-K ·
ZL-1503 MADTopline/data readoutStage not statedin the first half of 20278-K ·
ZL-6201Topline/data readoutPhase 1in the first half of 20278-K ·
Zocilurtatug pelitecan (DLLEVATE)Enrollment completionPhase 3in the first half of 20278-K ·
ElegrobartTopline/data readoutPhase 3in 20278-K ·
ZL-1222OtherPhase 1in 20278-K ·
ZL-1311 submissionPhase 1by year-end 20268-K ·

Source: ORION, orionbiotechai.com/company/ZLAB, data as of Oct 17, 2026
https://www.orionbiotechai.com/company/ZLAB

Nearest upcoming stated timing: ZL-1503 SAD · Topline/data readout · in the second half of 2026

SEC sources last checked .

Programs and stated timing

○ Quote matched to filing (not yet reviewed by founder) · ✓ Checked by founder.

ZL-1503 SAD

Matched

Topline/data readoutin the second half of 2026

Stage: Phase 1SEC filing · “Phase 1/1b”

Public float: $3,800,000,000 · as of · SEC filing

ZL-1503 (IL-13/IL-31Rα): Completed enrollment in the single ascending dose (SAD) portion of the Phase 1/1b study of ZL-1503 in healthy volunteers, with initial PK, PD, safety and immunogenicity data expected in the second half of 2026.

8-K · Filed · Last checked

Source details

Accession 0001628280-26-053791

SEC accepted the filing

ZL-1503 MAD

Matched

Topline/data readoutin the first half of 2027

Stage: Not stated

Public float: $3,800,000,000 · as of · SEC filing

Initial clinical data from the MAD portion expected in the first half of 2027.

SEC timing context:

ZL-1503 (IL-13/IL-31Rα) •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. •Continue enrollment in the MAD portion of the Phase 1/1b study in patients with atopic dermatitis.

8-K · Filed · Last checked

Source details

Accession 0001628280-26-053791

SEC accepted the filing

Topline/data readoutin the first half of 2027

Stage: Phase 1SEC filing · “Phase 1a”

Public float: $3,800,000,000 · as of · SEC filing

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.

8-K · Filed · Last checked

Source details

Accession 0001628280-26-053791

SEC accepted the filing

Zocilurtatug pelitecan (DLLEVATE)

Matched

Enrollment completionin the first half of 2027

Stage: Phase 3SEC filing · “Phase 3”

Public float: $3,800,000,000 · as of · SEC filing

Second-Line Plus ES-SCLC: Complete enrollment in the global pivotal Phase 3 DLLEVATE study in the first half of 2027 followed by a planned interim analysis with the potential to support a BLA submission for accelerated approval.

SEC timing context:

Zocilurtatug Pelitecan (zoci, DLL3-Targeting ADC; formerly ZL-1310)

8-K · Filed · Last checked

Source details

Accession 0001628280-26-053791

SEC accepted the filing

Elegrobart

Matched

Topline/data readoutin 2027

Stage: Phase 3SEC filing · “Phase 3”

Public float: $3,800,000,000 · as of · SEC filing

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

SEC timing context:

Elegrobart (Anti-IGF-1R, subcutaneous) •Zai Lab to complete enrollment in the Phase 3 registrational study for the treatment of thyroid eye disease in China in the third quarter of 2026.

8-K · Filed · Last checked

Source details

Accession 0001628280-26-053791

SEC accepted the filing

Otherin 2027

Stage: Phase 1SEC filing · “Phase 1”

Public float: $3,800,000,000 · as of · SEC filing

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

SEC timing context:

ZL-1222 (PD-1/IL-12)

8-K · Filed · Last checked

Source details

Accession 0001628280-26-053791

SEC accepted the filing

NDA/BLA submissionby year-end 2026

Stage: Phase 1SEC filing · “Phase 1”

Public float: $3,800,000,000 · as of · SEC filing

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.

SEC timing context:

ZL-1311 (MUC17/CD3)

8-K · Filed · Last checked

Source details

Accession 0001628280-26-053791

SEC accepted the filing

How this date was described over time

Company periods and sentences are quoted as written. A matching disclosure uses the SEC filing date for the same program and event type. As of .

Program / eventStated period and SEC wordingDisclosure in stated period
ElegrobartClinical resultsin 2027
“Zai Lab to provide topline results from the China Phase 3 registrational study in 2027.”

Filed · EX-99.1

Period not started

The stated period has not started yet, so there is nothing to compare.

ZL-1222Otherin 2027
“Submit an IND application in the U.S. and initiate a global Phase 1 study in 2027.”

Filed · EX-99.1

Period not started

The stated period has not started yet, so there is nothing to compare.

ZL-1311Submissionby year-end 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.”

Filed · EX-99.1

Not compared

ORION has no confirmed start and end dates for this wording, so it is not compared with filings.

ZL-1503 MADClinical resultsin the first half of 2027
“Initial clinical data from the MAD portion expected in the first half of 2027.”

Filed · EX-99.1

Period not started

The stated period has not started yet, so there is nothing to compare.

ZL-1503 SADClinical resultsin the second half of 2026
“ZL-1503 (IL-13/IL-31Rα): Completed enrollment in the single ascending dose (SAD) portion of the Phase 1/1b study of ZL-1503 in healthy volunteers, with initial PK, PD, safety and immunogenicity data expected in the second half of 2026.”

Filed · EX-99.1

Still within period

As of Oct 19, 2026

ZL-6201Clinical resultsin the first half of 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.”

Filed · EX-99.1

Period not started

The stated period has not started yet, so there is nothing to compare.

Zocilurtatug pelitecan (DLLEVATE)Enrollment completionin the first half of 2027
“Second-Line Plus ES-SCLC: Complete enrollment in the global pivotal Phase 3 DLLEVATE study in the first half of 2027 followed by a planned interim analysis with the potential to support a BLA submission for accelerated approval.”

Filed · EX-99.1

Period not started

The stated period has not started yet, so there is nothing to compare.

“Not compared” means ORION has not matched this wording against a complete set of SEC filings for its period. It says nothing either way about whether a matching filing exists. Wording without exact dates is not given calendar dates.

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Reading these records

First stated window
The timing wording in the earliest company statement located within the sources checked, quoted as written (for example “2H 2026”). An earlier statement may exist outside those sources.
Disclosure date
The date of the filing or company release that disclosed the readout. “None found” means no such disclosure was located in the sources checked. SEC filings were searched through the “SEC filings searched through” date shown.
1H, 2H, 1Q–4Q
First or second half, or first to fourth quarter, of the year named, as the company wrote it. Equivalent notations are compared together; the original wording stays visible.
SEC original
The filing as published on the SEC EDGAR system. “Company original” is the release on the company's own investor site.
Status
One of seven labels set by founder review of the original filings. Definitions: Methodology.

See ZLAB in the calendar · Review labels and methodology

Topline results are the main summary results of a clinical trial, released before the full data.A New Drug Application (NDA) or Biologics License Application (BLA) asks the FDA to approve a drug or biologic for sale.