Immunotherapy side effects under the microscope: MOTIVATE study tracks 150 patients
NCT ID NCT03447483
First seen Jun 27, 2026 · Last updated Sep 18, 2026 · Updated 2 times
Summary
This study followed 150 people with solid tumors who were starting immunotherapy (immune checkpoint inhibitors) as part of their regular care. Researchers collected data on side effects and asked patients to fill out questionnaires before each treatment. The goal was to better understand how and when side effects appear, not to test a new treatment.
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.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
150 people
The number who actually took part.
- Started
-
Apr 2018
- Finished
-
Jun 2020
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- 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: 1. Age \> or = 18 years old 2. Patient with a solid tumor whatever the organ 3. Patient receiving an Immune Checkpoint Inhibitor treatment 4. Patient starting first cycle of Immune Checkpoint Inhibitor treatment whatever the treatment line 5. Patient affiliated to the french social security system 6. Patient must provide written informed consent prior to inclusion in the study and any study-specific procedure Exclusion Criteria: 1. Patient who must receive a treatment other than Immune Checkpoint Inhibitor 2. Patient with contraindication to the use of a checkpoint inhibitor (e.g., auto immune disorders requiring an immunosuppressive therapy) 3. Pregnant or breastfeeding women 4. Any psychological, familial, geographical or sociological condition potentially preventing the medical follow-up and/or study procedures 5. Patient protected by law
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Solid tumor are added.
Genom att skicka in godkänner du våra Användarvillkor
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
-
CH ALBI
Albi, France
-
Ch Castres
Castres, France
-
Hopital Larrey
Toulouse, 31059, France
-
Institut Curie
Paris, 75005, France
-
Institut Regional Du Cancer de Montpellier (Icm)
Montpellier, 34298, France
-
Institut Universitaire Du Cancer de Toulouse - Oncopole
Toulouse, 31059, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- First human test of BI 4060107 aims to find safe dose for Hard-to-Treat tumors
- Can a new drug shield kidneys from chemotherapy damage?
- Mining Responders' tumors for clues to a universal cancer therapy
- Proton boost radiotherapy aims to hit large tumors harder while sparing healthy tissue
- New antibody aims to preserve immune checkpoint while fighting cancer
- Engineered immune cells target two markers on Hard-to-Treat tumors