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NCT05108519Recruiting

Complications and Clinical Response in Cancer Patients Treated With Anti-VEGF-Related Therapies

A Prospective Study Evaluating Complications and Clinical Response in Cancer Patients Treated With Anti-VEGF-Related Therapies

Source: ClinicalTrials.gov · Last updated 10 Aug 2026

Brief summary (registry, in English)

This study collects information about complications and clinical response in cancer patients treated with anti-VEGF-related therapies. This study aims to observe side effects that may happen to patients with advanced cancer who are treated with anti-VEGF related therapy. This may help doctors learn if there are any relationships between these side effects and how the disease may respond to treatment.

Status (registry)
Recruiting
Study type
Observational
Enrollment
170 (estimated)
First submitted
25 Oct 2021
Start date
8 Apr 2019
Primary completion date
2 Feb 2027
Lead sponsor
M.D. Anderson Cancer Center
NCT number
NCT05108519

What you commit to

  • Study type: Observational
  • Planned participants: 170
  • From 8 Apr 2019 to the primary completion date, 2 Feb 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • Patients must be able to understand and be willing to sign a written informed consent document
  • Patients must be receiving any anti-VEGF-related regimen in monotherapy or combination therapy

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
M D Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.