Evidence map›Paper›PMID 39494690›Full record

ArticleMolecular cancer therapeutics2025

Preclinical Characterization of XB002, an Anti-Tissue Factor Antibody-Drug Conjugate for the Treatment of Solid Tumors.

Seema Kantak, Raffaella Faggioni, Allen G Cai, Maryam M Bhatti, Jing Li, Inna Vainshtein, Jackie Cheng, Brian A Mendelsohn, Jacques Gaudreault, Thi-Sau Migone and 1 more

Abstract read
In one paragraph

Article in Molecular cancer therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Seema KantakDiscovery Biotherapeutics, Exelixis, Inc., Alameda, California.ORCID 0009-0007-8748-240X
Raffaella FaggioniClinical Pharmacology and Toxicology, Exelixis, Inc., Alameda, California.ORCID 0009-0007-1732-9311
Allen G CaiResearch, Iconic Therapeutics, South San Francisco, California.ORCID 0000-0003-3903-5166
Maryam M BhattiResearch, Iconic Therapeutics, South San Francisco, California.ORCID 0000-0002-5691-0893
Jing LiClinical Pharmacology and Toxicology, Exelixis, Inc., Alameda, California.ORCID 0009-0000-4569-9933
Inna VainshteinClinical Pharmacology and Toxicology, Exelixis, Inc., Alameda, California.ORCID 0009-0003-4473-5930
Jackie ChengClinical Pharmacology and Toxicology, Exelixis, Inc., Alameda, California.ORCID 0000-0001-9698-163X
Brian A MendelsohnDiscovery Biotherapeutics, Exelixis, Inc., Alameda, California.ORCID 0000-0002-6339-2377
Jacques GaudreaultResearch, Iconic Therapeutics, South San Francisco, California.ORCID 0009-0000-6391-131X
Thi-Sau MigoneResearch, Iconic Therapeutics, South San Francisco, California.ORCID 0000-0002-7744-0915
Jan-Willem TheunissenResearch, Iconic Therapeutics, South San Francisco, California.ORCID 0000-0002-1393-5732

Funding

Exelixis, Inc.
6 · The paper itself

Abstract

Tissue factor (TF) is overexpressed in various cancers and is typically associated with poor clinical outcomes. XB002 is an anti-TF antibody-drug conjugate designed to selectively deliver a cytotoxic payload to TF-expressing tumors while minimizing TF-related adverse events, particularly bleeding. The conjugate consists of a zovodotin linker-payload attached to a mAb (clone 25A3) that binds TF with high affinity (KD = 0.86 nmol/L). In vitro coagulation assays confirmed that 25A3 does not interfere with the clotting cascade; even at a concentration of 100 nmol/L, it did not affect the activation of coagulation factor X or thrombin generation. XB002 demonstrated efficient internalization in TF-expressing cancer cell lines, exhibiting potent cytotoxicity at subnanomolar concentrations. In the HPAF-II xenograft model, a regimen of XB002 (1.5 mg/kg, i.v.) administered once weekly for two weeks achieved complete tumor regression, with no detectable tumor growth up to five weeks after the second dose. In murine patient-derived xenograft models, a single dose of XB002 (10 mg/kg, i.v.) inhibited tumor growth across multiple cancer models, including bladder, cervical, gastric, head and neck squamous cell carcinoma, and non-small cell lung cancers. Remarkably, complete tumor regression was observed in the cervical cancer and head and neck squamous cell carcinoma models within 30 days of treatment. In nonhuman primate studies, XB002 demonstrated favorable pharmacokinetics with exposure in the desired therapeutic range and no signs of bleeding or neutropenia. Collectively, these data highlight XB002's broad-spectrum antitumor activity and strongly support its further clinical development.

Indexed as

Antibodies, MonoclonalImmunoconjugatesNeoplasmsThromboplastinAnimalsCell Line, TumorFemaleHumansMiceXenograft Model Antitumor AssaysAntibodies, MonoclonalImmunoconjugatesThromboplastin

Identifiers

PMID39494690
PMCPMC11791478

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.