Cancer drug opdivo qvantig under the microscope: who gets it and how?
NCT ID NCT07636863
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study reviewed medical records of 200 adults with cancer who received the drug nivolumab (Opdivo) either as an intravenous infusion or as a subcutaneous injection (Opdivo Qvantig) in community oncology clinics across the United States. The goal was to describe the types of patients receiving each form of the drug, how the treatments are used, and any injection- or infusion-related reactions or infections. This is an observational study, meaning it does not test a new treatment but rather gathers information on current real-world use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nivolumab (Opdivo) given as an intravenous infusion or as a subcutaneous injection combined with hyaluronidase
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
200 people
The number who actually took part.
- Started
-
Aug 2025
- Finished
-
Mar 2026
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adults with confirmed cancer diagnoses treated with intravenous (IV) nivolumab or subcutaneous (SC) nivolumab + hyaluronidase in U.S. community oncology practices.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Are ≥ 18 years of age at the index date * Have a confirmed cancer diagnosis * Received one of the following treatments: * Intravenous (IV) nivolumab * Subcutaneous (SC) nivolumab + hyaluronidase Exclusion Criteria: * Currently receiving a clinical trial therapy at index * Currently receiving treatment for another active concurrent primary cancer diagnosis * Received IV nivolumab or SC nivolumab + hyaluronidase off-label
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Florida Cancer Specialists & Research Institute
Fort Myers, Florida, 33916, United States
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