Weekly shot aims to melt away pounds in obesity fight
NCT ID NCT07822061
First seen Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time
Summary
Researchers are testing a new once-weekly injection called NNC0487-0111 in about 400 Japanese adults with overweight or obesity. Half the participants receive the drug and half receive a placebo, assigned by chance. The main goal is to measure how much body weight changes over the study. The trial also tracks waist circumference and safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an experimental once-weekly weight-loss injection called NNC0487-0111
- What this could lead to
- If it works, this could give Japanese adults with overweight or obesity another weekly injection option for weight loss.
- What could go wrong
- The trial may show the drug does not beat placebo, or side effects may outweigh the benefits. Results in Japanese participants may not apply to other groups.
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
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
About 400 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Sep 2026
- Expected to finish
-
Feb 2029
An estimate. End dates often move.
- 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.
- 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: * Male or female (sex at birth). * Age 18 years or above at the time of signing the informed consent. * For participants with T2D at screening (max 25%), the following inclusion criteria apply * Diagnosed with T2D ≥ 180 days before screening. * Haemoglobin A1c (HbA1c) 7.0 -10.0% (53-86 millimole per mole (mmol/mol) (both inclusive) as measured by the central laboratory at screening. * Treatment with lifestyle intervention, and/or with 0-3 marketed oral antidiabetic drugs (OADs) (Metformin, glinide, thiazolidinedione, sodium-glucose cotransporter-2 inhibitors, α-glucosidase inhibitors, imeglimin, or sulfonylureas (SU) as a single agent or in combination) according to local label. Treatment with OADs should be stable (same drug(s), dose and dosing frequency) before screening. * For participants with knee OA at screening (approximately 50 participants), the following inclusion criteria apply * Clinical diagnosis of knee OA (American College of Rheumatology criteria) with radio-graphic changes (Kellgren-Lawrence grades 2 to 3 as per central reading) in the target knee. Target knee joint is defined as most symptomatic knee at screening. If pain in knees is equal, the target knee joint will be the dominant leg. * Symptomatic knee OA with first appearance of pain in the target knee \> 90 days prior to screening and pain in the target knee for \> 15 days over the prior 30 days. * Willingness to complete a 72-hour washout period of analgesics before all visits in-volving WOMAC Osteoarthritis Index NRS 3.1 (24-hour) (WOMAC) questionnaire (acetaminophen 4 gram/day is allowed as rescue medication up until 24 hours before those visits). Exclusion Criteria: \- Treatment with glucagon-like-peptide-1 (GLP-1) receptor agonists (RA), dual GLP-1/gastric inhibitory peptide (GIP) RAs (or any other GLP-1 based treatment) or amylin analogues before screening. For participants without T2D at screening (including participants with and without knee OA), the following exclusion criteria apply in addition to criterion 1 (above): * HbA1c ≥ 6.5% (48 mmol/mol) as measured by the central laboratory at screening. * History of type 1 or type 2 diabetes mellitus. * For participants with T2D at screening, the following exclusion criteria apply in addition to criterion 1 (above): * Known hypoglycaemic unawareness as indicated by the investigator according to Clarke's questionnaire question 8. * Recurrent severe hypoglycaemic episodes within the last year as judged by the investigator. * Renal impairment with estimated Glomerular Filtration Rate (eGFR) \< 30 millilitre per minute per 1.73 m\^2, (2021 Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula (by creatinine)), at screening. * Participant with diabetic retinopathy or maculopathy who received treatment with retinal photocoagulation, vitrectomy or anti-Vascular Endothelial Growth Factor (anti-VEGF) within 180 days before screening or are expected to require treatment within 180 days after screening. * Diabetic retinopathy or maculopathy must be verified by an eye examination per-formed within 90 days before screening or in the period between screening and randomisation. * Pharmacological pupil-dilation is a requirement unless using a digital fundus photography camera specified for non-dilated examination. For participants with knee OA, the following exclusion criteria apply in addition to cri-teria 1-3 (above): * Any joint prosthesis or joint replacement in the target knee. * Arthroscopy or injections into the target knee within the last 90 days prior to screening. * Any other joint disease in the target knee including gout and pseudogout.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Knee osteoarthritis are added.
By submitting, you agree to our Terms of use
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The study's own enquiry address
This study publishes an address for enquiries. See it below .
-
The places running it
26 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Study contacts
-
Contact
Email: •••••@•••••
Locations
-
Akaicho Clinic_Internal medicine
RECRUITINGChiba-shi, Chiba, 260-0804, Japan
-
Clinical Research Hospital Tokyo_Internal medicine
RECRUITINGTokyo, 160-0004, Japan
-
Hayashi Diabetes Clinic_Internal Medicine and Diabetes Medicine
RECRUITINGChigasaki-shi, Kanagawa, Japan, 253-0044, Japan
-
Iwamoto Internal Medicine Clinic_Diabetes Internal Medicine
RECRUITINGKagawa, 765-0071, Japan
-
JCHO Kyushu Hospital_Department of Endocrinology and Metabolism
NOT_YET_RECRUITINGKitakyushu-shi, Fukuoka, 806-8501, Japan
-
Kuroda Orthopedic Clinic_Orthopedic Surgery and Internal Medicine
RECRUITINGFukuoka-shi, Fukuoka, 814-0165, Japan
-
Matsuba Clinic_Internal Medicine
NOT_YET_RECRUITINGKawasaki-shi, Kanagawa, Japan, 212 0024, Japan
-
Morimoto Clinic_Pain Clinic
NOT_YET_RECRUITINGOsaka-shi, Osaka, 530-0041, Japan
-
Motomachi Takatsuka Naika Clinic_Internal Medicine
NOT_YET_RECRUITINGKanagawa, 231-0023, Japan
-
Naka Kinen Clinic_Internal medicine
RECRUITINGIbaraki, 311-0113, Japan
-
National Hospital Organization Kyoto Medical Center_Diabetic Center
NOT_YET_RECRUITINGKyoto-shi, Kyoto, 612-8555, Japan
-
OCROM Clinic_Internal medicine
NOT_YET_RECRUITINGSuita-shi, Osaka, 565-0853, Japan
-
Seino Internal Medicine Clinic_Internal medicine
RECRUITINGKoriyama-shi, Fukushima, 963-8851, Japan
-
Shinsapporo Seiryou Hospital_General Clinical Department
RECRUITINGSapporo, Hokkaido, 004-0004, Japan
-
Suidoubashi Medical Clinic_Internal Medicine
RECRUITINGChiyoda-ku, Tokyo, 101-0065, Japan
-
TOSAKI Clinic for Diabetes and Endocrinology_Diabetes and Endocrinology
RECRUITINGAichi, 468-0009, Japan
-
Takai Internal Medicine Clinic_Internal Medicine
RECRUITINGKamakura-shi, Kanagawa, 247 0056, Japan
-
The University of Osaka Hospital_Metabolic Medicine
RECRUITINGOsaka, 565-0871, Japan
-
The University of Tokyo Hospital, Diabetes and Metabolic
NOT_YET_RECRUITINGBunkyo-ku, Tokyo, 113-8655, Japan
-
ToCROM Clinic_Internal Medicine
RECRUITINGTokyo, 160-0008, Japan
-
Tokuyama clinic_Diabetic internal medicine
NOT_YET_RECRUITINGChiba, 261-0004, Japan
-
Tokyo Asbo Clinic_Internal Medicine
RECRUITINGChuo-ku, Tokyo, 104-0031, Japan
-
Tokyo-Eki Center-building Clinic_Internal Medicine
NOT_YET_RECRUITINGTokyo, 103-0027, Japan
-
Tsuruma Kaneshiro Diabetes Clinic_Internal medicine
NOT_YET_RECRUITINGYamato-shi, Kanagawa, 242-0004, Japan
-
Yao Tokushukai General Hospital_Internal medicine
RECRUITINGYao City, Osaka, 581-0011, Japan
-
Yokohama Minoru Clinic_Internal medicine
NOT_YET_RECRUITINGKanagawa, 232-0064, Japan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- New pill takes aim at stubborn blood sugar
- Custom knee guides put to the test in obese patients
- Can a shot of your own blood ease arthritic knees?
- Gene therapy shots aim to save legs from amputation in diabetes
- 5,000 knee arthritis patients tracked to crack the treatment code
- A pill for obesity? early human trial puts MDR-001 to the test