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Zanzalintinib + atezolizumab

Research only

metastatic colorectal cancer

Published evidence

3 publications2 exact-program0 related5 context / correction notes

Review publications

Program details

Filing reports an extended review for zanzalintinib plus atezolizumab, with a March 3, 2027 target.

Program names
zanzalintinib / XL092
Modality
Small molecule
Indication
metastatic colorectal cancer
Associated trial
NCT05425940
FDA target
March 3, 2027Date-only guidance; not a trading cutoff.

Publications 3

Evidence is grouped by its relationship to this program.

Search PubMed

Publication notes explain the evidence behind this program. PubMed / NCBI data notice

Coverage & interpretation
  • The combination includes atezolizumab; it must not be represented as zanzalintinib monotherapy.
  • The protocol, results and erratum concern the same STELLAR-303 program and are not three independent trials.
  • Published erratum PMID 41241514 is included; its correction text was not retrieved.

Exact program / indication

2 records
Exact programhuman clinicalPMID 41130252

Zanzalintinib plus atezolizumab versus regorafenib in refractory colorectal cancer (STELLAR-303): a randomised, open-label, phase 3 trial.

Lancet (London, England) · 2025-10-20

STELLAR-303 compared zanzalintinib plus atezolizumab with regorafenib in a randomized phase 3 trial. The abstract reports an overall-survival benefit in the overall trial population and more grade 3 or worse treatment-related adverse events. PubMed links a correction that should be reviewed.

Program relevance

Phase 3 STELLAR-303 (NCT05425940) evaluates the exact zanzalintinib–atezolizumab combination in previously treated metastatic colorectal cancer.

Formulation / population: Oral zanzalintinib plus intravenous atezolizumab; not zanzalintinib monotherapy.

  • PubMed links a published erratum: PMID 41241514. Review the correction before interpreting results.

Journal Article / Randomized Controlled Trial / Clinical Trial, Phase III / Multicenter Study / Comparative Study / Research Support, Non-U.S. Gov't

Exact programTrial protocolPMID 39041200

STELLAR-303: randomized phase III study of zanzalintinib + atezolizumab in previously treated metastatic colorectal cancer.

Future oncology (London, England) · 2024-07-23

This publication describes the design and rationale of STELLAR-303, comparing zanzalintinib plus atezolizumab with regorafenib in previously treated metastatic colorectal cancer. It is a protocol publication, not a report of treatment outcomes.

Program relevance

The protocol describes the same STELLAR-303 combination trial; it is not an independent results study.

Formulation / population: Zanzalintinib plus atezolizumab in the same STELLAR-303 program as the results paper.

  • Trial protocol; not a results publication.
  • Do not count the protocol and results paper as independent trials.

Clinical Trial Protocol / Journal Article

Corrections, notices & retractions

1 record
Linked correctionPublication noticePMID 41241514

Department of Error.

Lancet (London, England) · 2025-11-15

Source metadata only: PubMed identifies a published correction and supplies no abstract. The correction text was not retrieved; no corrected values are asserted here.

Program relevance

PubMed links this published erratum to the STELLAR-303 results paper, PMID 41130252.

Formulation / population: Correction associated with the zanzalintinib–atezolizumab STELLAR-303 report.

  • Correction notice, not a separate clinical study.
  • No abstract supplied by PubMed.

Published Erratum

Sources

Publication and retrieval dates are shown separately. Market rules determine which evidence can resolve an outcome.

sec-filingwww.sec.gov
Filing reports an extended review for zanzalintinib plus atezolizumab, with a March 3, 2027 target.
Published
Sep 11, 2026
Retrieved
2026-10-30 02:09:48 UTC
sponsor-sciencewww.exelixis.com
Sponsor places zanzalintinib within its small-molecule discovery portfolio.
Published
Not supplied
Retrieved
2026-10-30 02:09:48 UTC
clinical-trial-registryclinicaltrials.gov
Registry identifies the associated compound, condition and sponsor; trial completion is separate from FDA action.
Published
Not supplied
Retrieved
2026-10-30 02:09:48 UTC

Research identity and publications do not establish regulatory approval, clinical suitability or an executable market. Read the limits