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Trial · NCT01813539

A Study of ARGX-110 in Participants With Advanced Malignancies

NCT01813539, Phase 1, Phase 2, Completed, OncoVerity, Inc.

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. A Study of ARGX-110 in Participants With Advanced Malignancies. Trials, record NCT01813539. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01813539

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A Study of ARGX-110 in Participants With Advanced Malignancies
NCT number
NCT01813539
Status
Completed
Phases
Phase 1, Phase 2
Enrollment
99 participants, actual
Lead sponsor
OncoVerity, Inc.
Conditions
Neoplasms
Interventions
ARGX-110
First posted
2013-03-19
Last updated
2023-08-09
Other registries' IDs
eudract:2012-005046-38

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of Participants with Dose Limiting Toxicity (DLT)21 daysDLT is defined as drug-related grade 3 or 4 clinical adverse event (AE) occurring during the 21 days (3 weeks) following the first dose of ARGX-110.
SecondaryPlasma Concentrations of ARGX-110Up to 2 yearsPlasma concentration of ARGX-110 will be assessed.
SecondaryBiomarkers (CD70 qPCR and sCD27) of ARGX-110 biological activityUp to 2 years
Biomarkers (CD70 quantitative polymerase chain reaction \[CD70 qPCR\] and soluble CD27 \[sCD27\]) will be measured in serum and on tumor samples to correlate systemic drug effects with AE and Tumor response.
SecondaryNumber of Participants who Achieve a Tumor ResponseUp to 2 yearsTumor response will be assessed according to RECIST.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
24492296DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01813539

GET https://conductscience.org/api/trials/v1/NCT01813539/registered