Evidence map›Paper›PMID 40444533›Full record

ArticleCancer research communications2025

A Phase 1 Safety Study of Evexomostat (SDX-7320) in Patients with Late-Stage Cancer: An Antiangiogenic, Insulin-Sensitizing Drug Conjugate Targeting METAP2.

Monica M Mita, Alain C Mita, Bradley J Carver, James M Shanahan, Benjamin A Mayes, Pierre J Dufour, David Browning, Alfred Anderson-Villaluz, John S Petersen, David J Turnquist and 1 more

Abstract readClinical Trial, Phase I
In one paragraph

Article in Cancer research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Monica M MitaHoag, Newport Beach, California.ORCID 0009-0004-8448-4854
Alain C MitaHoag, Newport Beach, California.ORCID 0009-0009-3260-4793
Bradley J CarverSynDevRx Inc., Cambridge, Massachusetts.ORCID 0009-0008-0081-4764
James M ShanahanSynDevRx Inc., Cambridge, Massachusetts.ORCID 0009-0006-1115-1519
Benjamin A MayesSynDevRx Inc., Cambridge, Massachusetts.ORCID 0009-0008-8762-6650
Pierre J DufourSynDevRx Inc., Cambridge, Massachusetts.ORCID 0009-0005-8476-1679
David BrowningSynDevRx Inc., Cambridge, Massachusetts.ORCID 0009-0001-1486-7022
Alfred Anderson-VillaluzNuvation Bio, San Francisco, California.ORCID 0009-0007-3901-5831
John S PetersenGlyscend Therapeutics, Lowell, Massachusetts.ORCID 0009-0007-6006-8700
David J TurnquistHemavant Sciences, New York, New York.ORCID 0009-0000-5423-3174
Peter CorneliusSynDevRx Inc., Cambridge, Massachusetts.ORCID 0009-0000-9448-3792

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate the safety and tolerability of evexomostat (SDX-7320) in patients with late-stage cancer. PATIENTS AND

methodsThis phase 1 dose-escalation safety study used an accelerated titration followed by a 3 + 3 design on 7- or 14-day administration, with dose expansion at the recommended phase 2 dose in 32 patients with late-stage, solid tumors. Measurements included standard assessments of safety, tolerability, target engagement in whole blood, plasma levels of protein biomarkers, and drug exposure. Tumor response was measured using RECIST v.1.1.

resultsThirty-two patients were dosed with evexomostat (SDX-7320), starting at 1.7 mg/m2 once per week and escalated to 65 mg/m2 (once every 2 weeks, 28 days/cycle). Dose escalation and expansion confirmed the maximum tolerated dose at 49 mg/m2 once every 2 weeks with reversible thrombocytopenia as the dose-limiting toxicity. Most treatment-emergent adverse events were of grade 1 or 2 in severity and nonserious, with no grade 5 adverse events. Eighty percent of patients (n = 20/25 evaluable) had stable disease, and the average treatment duration was 87 days (3.1 cycles). Key angiogenic biomarkers VEGF-C and bFGF (FGF2) improved in response to evexomostat. Patients with baseline insulin resistance (i.e., fasting insulin >20 µU/mL; n = 11) exhibited significant decreased fasting insulin after treatment. Decreases in leptin were observed in 27/31 patients (87%), whereas adiponectin increased in 28/31 patients (90%). Plasma lipid profiles showed increased high-density lipoprotein (HDL) and decreased low-density lipoprotein (LDL) cholesterol.

conclusionsEvexomostat (SDX-7320) was well-tolerated with prolonged stable disease and metastatic control in an open-label, phase I safety study. Improvements were observed in angiogenic and metabolic biomarkers. SIGNIFICANCE: Obesity and insulin resistance are known to promote tumor growth and accelerate the mortality of patients with cancer. Evexomostat is a novel antiangiogenic and antimetastatic drug candidate which also has insulin-sensitizing and antiobesity properties that is being developed for use in combination with standard-of-care therapies for obese patients with cancer.

Indexed as

Angiogenesis InhibitorsNeoplasmsAdultAgedFemaleHumansImidazolesInsulin ResistanceMaleMaximum Tolerated DoseMiddle AgedNeoplasm StagingPyrazines3-(8-amino-1-(2-phenylquinolin-7-yl)imidazo(1,5-a)pyrazin-3-yl)-1-methylcyclobutanolAngiogenesis InhibitorsImidazolesPyrazines

Identifiers

PMID40444533
PMCPMC12183619

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Registered trials

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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 OpenQuestion graph.