Obesity & OverweightREAL-BODYNCT07776678
Redefining Evaluation of Adiposity and Leanness: Broadening Objective Diagnostics for Obesity
An observational study of Obesity & Overweight, run by Foundation for the National Institutes of Health at 3 sites in United States.
Trial summary
The purpose of this study is to evaluate body composition across a variety of medical, professional, and commercial devices, including: bioelectrical impedance analysis (BIA) devices, 3-dimensional optical imaging (3DO), manual anthropometry measurements, dual-energy X-ray absorptiometry (DXA), magnetic resonance… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Obesity & Overweight
- How many people
- 300 participants
- Where
- 3 sitesUnited States
- Study dates
- 29 Jun 2026to 30 Mar 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Adult, Older adult
Study population: A diverse sample of adults will be recruited for participation in the US. Stratification will occur based on sex and BMI, with additional targets to promote recruitment of a variety of ages and adequate representation of racial and ethnic categories. For race and ethnicity, the goal will be to obtain a distribution approximately equal to the demographics of the United States, with selective oversampling employed as needed. For BMI, the following percentages will be used as approximate goals for the sample (18.50-19.99, None; 20.00-24.99, 20%; 25.00-29.99, 35%; 30.00-34.99, 25%; 35.00-39.99, 13.30%; 40.00-44.99, 6.70%; ≥45, None). However, the distribution of BMI and other demographic characteristics will be monitored as the study progresses in case adjustment is needed.
Who may be able to join
- Being willing to provide written informed consent prior to participation Being willing to complete the study visits and comply with the study procedures
- Being willing to travel to the various study locations for On-site, DXA, MRI, and Phlebotomy visits
- Being willing to change into appropriate form-fitting clothing for 3DO assessments and/or appropriate gowns for DXA and MRI imaging
- Must have a BMI within the range of 18.5 - 45 kg/m2
- Being willing to refrain from all food, drink, and substances for 8 hours prior to the On-site visit(s) and phlebotomy visit
- Being willing to refrain from all food, drink, and substances for 4 hours prior to the DXA and MRI scan visits
Show all 9Show fewer
- Being willing to refrain from any exercise or vigorous physical activity for 24 hours prior to all visits
- Stable weight (no more than 5 kg change) for 3 months prior to screening
- If recruited in the Phoenix, AZ area, participants must be willing to drive yourself to the Phoenix Office location for the On-site Visits 1 and 2 (if applicable) located at the Exponent Phoenix Office.
Who cannot join
- Being pregnant or attempting to become pregnant
- Having medical implants, such as a pacemaker or metal joint replacements, or other metal implants contraindicated for MRI
- Cosmetic implants, such as breast implants
- Having a height greater than DXA scanning limit (77 inches)
- Having a body weight greater than indicated for the equipment (400 lbs)
- Prior amputation or major body-altering surgery that could invalidate body composition estimates
Show all 11Show fewer
- Having claustrophobia or a history of claustrophobia
- Known HIV infection
- Known Lipodystrophy
- Known hydration abnormality (e.g., significant edema, end-stage renal disease, end-stage liver disease)
- Severe illness or life-threatening conditions such as end-stage kidney, liver, lung disease, NYHA III-IV heart failure, or active malignancy
Trial locations and contacts
3 sites in 1 country. Contact the study team or a site near you to ask about taking part.
United States3 sites, 3 recruiting
- Recruiting
Exponent Boston
Boston, Massachusetts, 01760
Ariel Dowling, 650-688-4070, bodycompstudy@exponent.com
- Recruiting
Exponent Menlo Park
Menlo Park, California, 94025
Erica Lively Site Lead, PhD, 208-310-9415, elively@exponent.com
- Recruiting
Exponent Phoenix
Phoenix, Arizona, 85027
Marysol Luna, 650-688-4070, bodycompstudy@exponent.com
About this study
Official title: Redefining Evaluation of Adiposity and Leanness: Broadening Objective Diagnostics for Obesity (REAL-BODY)
The purpose of this study is to evaluate body composition across a variety of medical, professional, and commercial devices, including: bioelectrical impedance analysis (BIA) devices, 3-dimensional optical imaging (3DO), manual anthropometry measurements, dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI), and blood tests. The secondary study purpose is to compare body composition measurements from BIA devices, 3DO, and manual anthropometry measurements within a 1-week period for a subset of the study population.
The study plans to enroll 300 healthy (having no life-threatening conditions or diseases; male and female) participants, 18 years of age or older.
Read the detailed description
Obesity is a disease of excess and abnormal distribution of adipose tissue. Even though negative metabolic outcomes of obesity are driven by adipose tissue, investigators still use body weight (comprised of both fat and fat-free mass) in the calculation of body mass index (weight in kg divided by height in meters squared) to define, subclassify and monitor treatment in people with obesity. Despite this traditional focus on body weight, body composition is an important consideration in the management of people with obesity.
Clinical trials and clinical research often use DXA and MRI to quantify changes in body composition; however these methods are expensive and not easily implemented. It is desirable to monitor fat mass and other body composition outcomes in individuals with obesity taking weight loss medications as well as when new weight management therapeutic drugs are developed.
Most weight loss medications are associated with loss of both fat mass and fat-free mass with the "quality of weight loss" defined as the proportion of weight lost as fat mass, equal to 60-75%. Recognizing that loss of fat-free mass during weight loss is undesirable, several companies are developing lean mass preserving weight loss agents. For these agents, stepping on a weight scale will no longer be an accurate measure of benefit; loss in fat is offset by gains in lean, rendering body weight changes as an inaccurate measure of weight loss quality. Therefore, the application of body composition measurements will be required for patients, physicians, and payors to monitor treatment in people with obesity. In order for this to occur, investigators need scalable body composition measurements for fat mass.
Bioelectrical impedance analysis (BIA) offers a more scalable approach as the time, cost and footprint of BIA devices make them appropriate for a physician's office and for clinical research trials. Traditionally, BIA devices have been deemed to possess insufficient accuracy for body composition quantification. While this decreased accuracy was an obstacle for first generation weight loss medications with less weight loss, it is possible that with the newer generation of weight loss medications that confer greater weight loss, BIA may be adequate to measure changes in body composition occurring over time in individuals losing weight. Additionally, notable technological innovation has occurred in the field of bioimpedance, with several new devices possessing improved hardware and software as compared to previously evaluated analyzers. As such, these devices are expected to outperform traditional BIA systems.
Other accessible technologies that are practical to apply in clinical research and practice have appeared in recent publications. These include three-dimensional optical systems (3DO) housed in smartphones and multi-omics blood tests capable of estimating various body compartments. To the extent that BIA and these newer technologies can serve as useful sufficiently reproducible phenotypic measures of a person's body composition remains largely unknown. In addition to the dichotomy of fat mass vs fat-free mass, not all fat mass is created equal. Superficial or subcutaneous fat mass is thought to be metabolically healthy whereas visceral central fat is thought to be metabolically unhealthy. Furthermore, visceral fat is associated with long-term morbidity and mortality. Therefore, another dimension of body composition is the proportion of fat in the visceral vs subcutaneous compartments.
Currently, MRI is the gold standard method to measure visceral fat. Some BIA analyzers provide estimations of visceral fat, and digital anthropometry derived from 3D scanning can also be used in visceral fat estimation equations. As such, an additional goal of this project is to determine if visceral fat can be accurately estimated in the real-world using BIA or 3DO. Currently there are two major manufacturers of DXA devices, Hologic and General Electric (GE). Accuracy and precision data for body composition measures using DXA have been published. For BIA, there are several different manufacturers including InBody, Tanita, Seca, and Impedimed. Likewise, several companies produce 3DO smartphone systems, and one company provides multi omics blood evaluations for body composition. It is not known which of these devices and measurement platforms (if any) have adequate accuracy to measure body composition. The overall goal of this project is to bring measurement of body composition to the real world to improve the diagnosis, classification, and monitoring of treatment in people with obesity, both in clinical research trials and medical practice. Adipose or fat mass needs to become a new "vital sign." This project could have a large impact on the treatment of people with obesity. Accurate implementation of body composition analysis in the real world could lead to the development of treatment goals for obesity based on either total fat mass and/or visceral fat mass.
- Conditions
- Obesity & Overweight
- Keywords
- Body Composition
- Medical subject headings
- Obesity, Overweight
What is being measured
The primary outcome is the main question the study is designed to answer.
Modality-reference agreement for total fat mass (kg)
Agreement between bioimpedance and 3-dimensional optical imaging derived estimates of total fat mass and DXA-derived reference measurements.
Measured: 4 Weeks
Modality-reference agreement for fat-free mass (kg)
Agreement between bioimpedance and 3-dimensional optical imaging derived estimates of fat-free mass and DXA-derived reference measurements.
Measured: 4 Weeks
Modality-reference agreement for percent body fat (%)
Agreement between bioimpedance and 3-dimensional optical imaging derived estimates of percent body fat and DXA-derived reference measurements.
Measured: 4 Weeks
Modality-reference agreement for visceral adipose tissue (VAT; kg or volume)
Agreement between bioimpedance and 3-dimensional optical imaging derived estimates of visceral adipose tissue and MRI-derived reference measurements.
Measured: 4 Weeks
Secondary outcomes (11)
Agreement of blood-based proteomics-derived fat-free mass with DXA-derived fat-free mass (kg)
Agreement between blood-based proteomics-derived fat-free mass and DXA-derived fat-free mass, assessed using the prespecified agreement analyses.
Measured: 4 Weeks
Agreement of blood-based proteomics-derived total fat mass with DXA-derived total fat mass (kg)
Description: Agreement between blood-based proteomics-derived total fat mass and DXA-derived total fat mass, assessed using the prespecified agreement analyses.
Measured: 4 Weeks
Agreement of blood-based proteomics-derived percent body fat with DXA-derived percent body fat (%)
Agreement between blood-based proteomics-derived percent body fat and DXA-derived percent body fat, assessed using the prespecified agreement analyses.
Measured: 4 Weeks
Agreement of blood-based proteomics-derived visceral adipose tissue with MRI-derived visceral adipose tissue
Agreement between blood-based proteomics-derived visceral adipose tissue and MRI-derived visceral adipose tissue, assessed using the prespecified agreement analyses
Measured: 4 Weeks
Obesity and elevated visceral adipose tissue classification
Classification performance of bioimpedance (BIA), 3-dimenisonal optics imaging (3DO), and blood-based methods for obesity and elevated visceral adipose tissue (VAT) status, assessed using area under the receiver operating characteristic curve (AUC) based on prespecified thresholds.
Measured: 4 Weeks
Regression-based assessment of demographic and anthropometric effects on modality-reference measurement error
Regression models will be used to evaluate the effects of prespecified demographic and anthropometric covariates, including age, sex, and BMI, on measurement error between candidate body composition methods and the corresponding DXA or MRI reference method.
Measured: 4 Weeks
Between-day reliability of BIA measurements assessed by intraclass correlation coefficient (ICC)
Intraclass correlation coefficients with 95% confidence intervals will be calculated for repeated BIA measurements obtained during the protocol-specified repeat-visit window of 2-7 days.
Measured: 1 Week
Between-day reliability of 3DO measurements assessed by intraclass correlation coefficient (ICC)
Intraclass correlation coefficients with 95% confidence intervals will be calculated for repeated 3DO measurements obtained during the protocol-specified visit window of 2-7 days.
Measured: 1 Week
Between-day reliability of BIA measurements assessed by technical error of measurement (TEM)
Technical error of measurement will be calculated for repeated BIA measurements obtained during the protocol-specified repeat-visit window of 2-7 days.
Measured: 1 Week
Between-day reliability of 3DO measurements assessed by technical error of measurement (TEM)
Technical error of measurement will be calculated for repeated 3DO measurements obtained during the protocol-specified repeat-visit window of 2-7 days
Measured: 1 Week
Exploratory predictive performance of novel 3DO-derived geometric and anthropometric features for visceral adipose tissue
Exploratory models incorporating 3DO-derived geometric and anthropometric features will be evaluated for estimation of visceral adipose tissue relative to MRI-derived reference measurements using regression-based predictive performance measures.
Measured: 4 Weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Aug 2026
- Study start29 Jun 2026
- Primary completion30 Nov 2026 (estimated)
- Study completion30 Mar 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Obesity & OverweightStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 300 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Foundation for the National Institutes of Health
- Sponsor type
- University, hospital or other
- Collaborators
- Exponent, Inc., Pennington Biomedical Research Center, Texas Tech University
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07776678
- Sponsor's protocol ID
- 00329050
- Acronym
- REAL-BODY
- Status last verified
- Oct 2026
- First submitted
- 14 Jul 2026
- Last updated
- 26 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Redefining Evaluation of Adiposity and Leanness: Broadening Objective Diagnostics for Obesity (REAL-BODY)
- ClinicalTrials.gov ID
- NCT07776678
- Acronym / sponsor ID
- REAL-BODY / 00329050
- Conditions
- Obesity & Overweight
- Keywords
- Body Composition
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- Foundation for the National Institutes of HealthUniversity, hospital or other
- Collaborators
- Exponent, Inc., Pennington Biomedical Research Center, Texas Tech University
- Study start
- 29 Jun 2026 (actual)
- Primary completion
- 30 Nov 2026 (estimated)
- Study completion
- 30 Mar 2027 (estimated)
- First posted
- 20 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to evaluate body composition across a variety of medical, professional, and commercial devices, including: bioelectrical impedance analysis (BIA) devices, 3-dimensional optical imaging (3DO), manual anthropometry measurements, dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI), and blood tests. The secondary study purpose is to compare body composition measurements from BIA devices, 3DO, and manual anthropometry measurements within a 1-week period for a subset of the study population.
The study plans to enroll 300 healthy (having no life-threatening conditions or diseases; male and female) participants, 18 years of age or older.
Detailed description
Obesity is a disease of excess and abnormal distribution of adipose tissue. Even though negative metabolic outcomes of obesity are driven by adipose tissue, investigators still use body weight (comprised of both fat and fat-free mass) in the calculation of body mass index (weight in kg divided by height in meters squared) to define, subclassify and monitor treatment in people with obesity. Despite this traditional focus on body weight, body composition is an important consideration in the management of people with obesity.
Clinical trials and clinical research often use DXA and MRI to quantify changes in body composition; however these methods are expensive and not easily implemented. It is desirable to monitor fat mass and other body composition outcomes in individuals with obesity taking weight loss medications as well as when new weight management therapeutic drugs are developed.
Most weight loss medications are associated with loss of both fat mass and fat-free mass with the "quality of weight loss" defined as the proportion of weight lost as fat mass, equal to 60-75%. Recognizing that loss of fat-free mass during weight loss is undesirable, several companies are developing lean mass preserving weight loss agents. For these agents, stepping on a weight scale will no longer be an accurate measure of benefit; loss in fat is offset by gains in lean, rendering body weight changes as an inaccurate measure of weight loss quality. Therefore, the application of body composition measurements will be required for patients, physicians, and payors to monitor treatment in people with obesity. In order for this to occur, investigators need scalable body composition measurements for fat mass.
Bioelectrical impedance analysis (BIA) offers a more scalable approach as the time, cost and footprint of BIA devices make them appropriate for a physician's office and for clinical research trials. Traditionally, BIA devices have been deemed to possess insufficient accuracy for body composition quantification. While this decreased accuracy was an obstacle for first generation weight loss medications with less weight loss, it is possible that with the newer generation of weight loss medications that confer greater weight loss, BIA may be adequate to measure changes in body composition occurring over time in individuals losing weight. Additionally, notable technological innovation has occurred in the field of bioimpedance, with several new devices possessing improved hardware and software as compared to previously evaluated analyzers. As such, these devices are expected to outperform traditional BIA systems.
Other accessible technologies that are practical to apply in clinical research and practice have appeared in recent publications. These include three-dimensional optical systems (3DO) housed in smartphones and multi-omics blood tests capable of estimating various body compartments. To the extent that BIA and these newer technologies can serve as useful sufficiently reproducible phenotypic measures of a person's body composition remains largely unknown. In addition to the dichotomy of fat mass vs fat-free mass, not all fat mass is created equal. Superficial or subcutaneous fat mass is thought to be metabolically healthy whereas visceral central fat is thought to be metabolically unhealthy. Furthermore, visceral fat is associated with long-term morbidity and mortality. Therefore, another dimension of body composition is the proportion of fat in the visceral vs subcutaneous compartments.
Currently, MRI is the gold standard method to measure visceral fat. Some BIA analyzers provide estimations of visceral fat, and digital anthropometry derived from 3D scanning can also be used in visceral fat estimation equations. As such, an additional goal of this project is to determine if visceral fat can be accurately estimated in the real-world using BIA or 3DO. Currently there are two major manufacturers of DXA devices, Hologic and General Electric (GE). Accuracy and precision data for body composition measures using DXA have been published. For BIA, there are several different manufacturers including InBody, Tanita, Seca, and Impedimed. Likewise, several companies produce 3DO smartphone systems, and one company provides multi omics blood evaluations for body composition. It is not known which of these devices and measurement platforms (if any) have adequate accuracy to measure body composition. The overall goal of this project is to bring measurement of body composition to the real world to improve the diagnosis, classification, and monitoring of treatment in people with obesity, both in clinical research trials and medical practice. Adipose or fat mass needs to become a new "vital sign." This project could have a large impact on the treatment of people with obesity. Accurate implementation of body composition analysis in the real world could lead to the development of treatment goals for obesity based on either total fat mass and/or visceral fat mass.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- A diverse sample of adults will be recruited for participation in the US. Stratification will occur based on sex and BMI, with additional targets to promote recruitment of a variety of ages and adequate representation of racial and ethnic categories. For race and ethnicity, the goal will be to obtain a distribution approximately equal to the demographics of the United States, with selective oversampling employed as needed. For BMI, the following percentages will be used as approximate goals for the sample (18.50-19.99, None; 20.00-24.99, 20%; 25.00-29.99, 35%; 30.00-34.99, 25%; 35.00-39.99, 13.30%; 40.00-44.99, 6.70%; ≥45, None). However, the distribution of BMI and other demographic characteristics will be monitored as the study progresses in case adjustment is needed.
Key inclusion criteria (9 listed)
- Being willing to provide written informed consent prior to participation Being willing to complete the study visits and comply with the study procedures
- Being willing to travel to the various study locations for On-site, DXA, MRI, and Phlebotomy visits
- Being willing to change into appropriate form-fitting clothing for 3DO assessments and/or appropriate gowns for DXA and MRI imaging
- Must have a BMI within the range of 18.5 - 45 kg/m2
- Being willing to refrain from all food, drink, and substances for 8 hours prior to the On-site visit(s) and phlebotomy visit
Key exclusion criteria (11 listed)
- Being pregnant or attempting to become pregnant
- Having medical implants, such as a pacemaker or metal joint replacements, or other metal implants contraindicated for MRI
- Cosmetic implants, such as breast implants
- Having a height greater than DXA scanning limit (77 inches)
- Having a body weight greater than indicated for the equipment (400 lbs)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Modality-reference agreement for total fat mass (kg)
Time frame: 4 Weeks
Agreement between bioimpedance and 3-dimensional optical imaging derived estimates of total fat mass and DXA-derived reference measurements.
Modality-reference agreement for fat-free mass (kg)
Time frame: 4 Weeks
Agreement between bioimpedance and 3-dimensional optical imaging derived estimates of fat-free mass and DXA-derived reference measurements.
Modality-reference agreement for percent body fat (%)
Time frame: 4 Weeks
Agreement between bioimpedance and 3-dimensional optical imaging derived estimates of percent body fat and DXA-derived reference measurements.
Modality-reference agreement for visceral adipose tissue (VAT; kg or volume)
Time frame: 4 Weeks
Agreement between bioimpedance and 3-dimensional optical imaging derived estimates of visceral adipose tissue and MRI-derived reference measurements.
11 secondary outcomes
Agreement of blood-based proteomics-derived fat-free mass with DXA-derived fat-free mass (kg)
Time frame: 4 Weeks
Agreement of blood-based proteomics-derived total fat mass with DXA-derived total fat mass (kg)
Time frame: 4 Weeks
Agreement of blood-based proteomics-derived percent body fat with DXA-derived percent body fat (%)
Time frame: 4 Weeks
Agreement of blood-based proteomics-derived visceral adipose tissue with MRI-derived visceral adipose tissue
Time frame: 4 Weeks
Obesity and elevated visceral adipose tissue classification
Time frame: 4 Weeks
Regression-based assessment of demographic and anthropometric effects on modality-reference measurement error
Time frame: 4 Weeks
Between-day reliability of BIA measurements assessed by intraclass correlation coefficient (ICC)
Time frame: 1 Week
Between-day reliability of 3DO measurements assessed by intraclass correlation coefficient (ICC)
Time frame: 1 Week
Between-day reliability of BIA measurements assessed by technical error of measurement (TEM)
Time frame: 1 Week
Between-day reliability of 3DO measurements assessed by technical error of measurement (TEM)
Time frame: 1 Week
Exploratory predictive performance of novel 3DO-derived geometric and anthropometric features for visceral adipose tissue
Time frame: 4 Weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Oct 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Obesity & Overweight, run by Foundation for the National Institutes of Health at 3 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 26 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Steven Heymsfield, MD (650-688-4070, bodycompstudy@exponent.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Modality-reference agreement for total fat mass (kg) (time frame: 4 Weeks). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Oct 2026.