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SarcopeniaPhase 2SARA-INTNCT03452488

A Double-blind, Placebo-controlled, Randomized INTerventional Clinical Trial (SARA-INT)

A Phase 2 study testing BIO101 in people with Sarcopenia and Gait Disorders in Old Age, run by Biophytis at 22 sites in 2 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The main objective of the study is to evaluate the effect of two daily doses of BIO101 versus placebo on mobility function as measured by gait speed using the 400MW test. The absolute change from baseline in meters/second observed in each treatment group at 6 Month was compared to the placebo group. Read more about this study

Who is it for?
Ages 65 years and older
What is being tested?
BIO101
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
233 participants
Where
22 sitesin 2 countries
Study dates
7 Feb 2017to 26 Apr 2020
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

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 65 years and older
  • All sexes
  • No healthy volunteers
  • Older adult

Who may be able to join

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Male or female, aged ≥ 65 years and living in the community, reporting loss of physical function over the last 6-12 months
  • Short Physical Performance Battery (SPPB) score ≤ 8
  • ALM/BMI < 0.789 in men and 0.512 in women, or ALM < 19.75kg in men and <15.02kg in women, as measured by DEXA scan
  • Ability to take oral medication and be willing to adhere to the study intervention regimen.
  • Agreement to adhere to Lifestyle Considerations throughout study duration
  • In the US, women and members of minority groups must be included in accordance with the NIH Policy on Inclusion of Women and Minorities as Participants In Research Involving Human participants.

Who cannot join

  • Current use of anabolic drugs (e.g. testosterone); current use of Erythropoietin; current use of corticosteroid agents (except local administration route, like eye drops or dermatologic formulations)
  • Non-menopaused women (however ongoing replacement hormonal treatment is not an exclusion criterion)
  • Known allergic reactions to components of the investigational drug.
  • Treatment with another investigational drug or other intervention within three months
  • Unable to understand and perform the functional tests, as judged by the Investigator
  • Inability to perform the 400MW test within 15 minutes
Show all 19Show fewer
  • Clinical conditions:
  • Current diagnosis of major psychiatric disorders.
  • Alcohol abuse or dependence
  • Severe arthritis
  • Cancer requiring active treatment (cancer treated with chemotherapy, or radiotherapy and currently on remission is not an exclusion criterion)
  • Lung disease requiring regular use of supplemental oxygen
  • Inflammatory conditions requiring regular use of oral or parenteral corticosteroid agents
  • Severe cardiovascular disease (including New York Heart Association [NYHA] class III or IV congestive heart failure, clinically significant valvular disease, history of cardiac arrest, presence of an implantable defibrillator, or uncontrolled angina)
  • Parkinson's disease or other progressive neurological disorder
  • Renal disease requiring dialysis, or known renal insufficiency (moderate or severe reduction in GFR≤30 ml/min/1.73 m2)
  • Chest pain, severe shortness of breath, or occurrence of other safety concerns during the baseline functional tests 400-meter walk test or 6MWT
  • History or active signs or symptoms of gallbladder/biliary disease (e.g. previous episodes of cholestasis/biliary tract obstruction, cholelithiasis, cholecystitis, etc.). Of note, history of cholecystectomy and no active biliary signs or symptoms, is not an exclusion criterion.
  • Current physical/rehabilitation therapy (except for passive physical therapy. However, this should not be initiated the week before an evaluation visit and once started, it should be maintained over the study duration).

Trial locations and contacts

22 sites in 2 countries.

22 sites in 2 countries

United States19 sites
  • New Mexico Clinical Research & Osteoporosis Center

    Albuquerque, New Mexico, 87106

  • Tekton Research

    Austin, Texas, 78745

  • Advanced Clinical Research

    Banning, California, 92221

  • Pennington Biomedical Research Center

    Baton Rouge, Louisiana, 70808

  • Jean Mayer USDA Human Nutrition research Center on Aging Tufts University

    Boston, Massachusetts, 02111

  • Institut On Aging

    Gainesville, Florida, 32611

  • SC Clinical Research, Inc

    Garden Grove, California, 92844

  • Medical Center

    Houston, Texas, 77030

  • Jax-Ascent University of Florida

    Jacksonville, Florida, 32209

  • PANAX Clinical Research

    Miami Lakes, Florida, 33014

  • Columbia University

    New York, New York, 10032

  • Clinical Research of Central Florida

    Plant City, Florida, 33563

  • Science Advancing Medicine Clinical Research Center

    San Antonio, Texas, 78229

  • The University of Texas Health Science Center at San Antonio

    San Antonio, Texas, 78245

  • California Research Foundation

    San Diego, California, 92123

  • Advanced Clinical Research

    West Jordan, Utah, 84088

  • PMJ Research of Wilmington

    Wilmington, North Carolina, 28401

  • Bowman Gray Center for Medical Education-of- Wake Forest School of Medicine

    Winston-Salem, North Carolina, 27101

  • Tekton Research

    Yukon, Oklahoma, 73099

Other trials in United States

Belgium3 sites
  • Vrije Universiteit Brussel

    Brussels, 1090

  • Universitaire Ziekenhuizen (UZ) Leuven - Gasthuisberg - Centrum voor metabole botziekten

    Leuven, 3000

  • Université de Liège

    Liège, 4020

Other trials in Belgium

About this study

Official title: Safety and Efficacy of BIO-101 175 mg b.i.d. and 350 mg b.i.d. 26-week Oral Administration to Patients Suffering From Age-related SARcopenia, Including Sarcopenic Obesity, Aged ≥65 Years and at Risk of Mobility Disability

The main objective of the study is to evaluate the effect of two daily doses of BIO101 versus placebo on mobility function as measured by gait speed using the 400MW test. The absolute change from baseline in meters/second observed in each treatment group at 6 Month was compared to the placebo group. Due to the Covid pandemic >50% of data at endpoint was missing, which may have affected the ability of the study to deliver the expected results. Additionally, although the planned duration of treatment was 6 months, it was extended up to 9 months for some participants as a result of the pandemic.

Read the detailed description

The aim of this phase 2 double-blind, placebo-controlled, randomized interventional clinical trial (SARA-INT) is to evaluate the safety and efficacy of BIO-101 175 mg b.i.d. and 350 mg b.i.d. 9 months oral administration to participants suffering from age-related sarcopenia, including sarcopenic obesity, aged ≥65 years and at risk of mobility disability. There are 3-arms (2 doses versus placebo). This comparative clinical trial evaluated the effects up to 9 month treatment duration, based on the hypothesis that physical function of sarcopenic, older participants with an initial degree of mobility disability (SPPB) may be improved by BIO101.

Included participants were randomized in a 1:1:1 ratio, to one of the 3 arms of treatment in a blinded manner. The randomization was stratified by gender and by center. Based on absence of long-term toxicology data, the investigational drug exposure was initially capped at 6 months.

Being tested
BIO101, Placebo
Keywords
Sarcopenia, Sarcopenic Obesity, 6-minute walking distance, 400 meters walking test, BIO101, Short Physical Performance Battery, Appendicular lean mass
Medical subject headings
Sarcopenia, Muscle Weakness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BIO101Drug

    Also called 20 hydroxyecdysone (20E)

    Oral capsules

  • PlaceboDrug

    Oral capsules

Study groups in NCT03452488
Study groupRoleWhat they receive
PlaceboPlacebo comparatorPlacebo was taken orally, two capsules twice daily (BID), 12 hours apart, up to 9 months.
Receives: Drug: Placebo
175mg BIO101ExperimentalBIO101 was taken orally, two capsules BID, 12 hours apart, up to 9 months.
Receives: Drug: BIO101
350mg BIO101ExperimentalBIO101 was taken orally, two capsules BID, 12 hours apart, up to 9 months.
Receives: Drug: BIO101

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change From Baseline to 6 Months in Gait Speed for 400 Meter Walking (MW) Test

    Gait speed was measured using the 400 MW test, which measured how long it took the participant to walk a distance of 400 meters. Missing data imputed using adjusted Bayesian Multiple Imputation (MI) methods for Non-Completers who failed to perform the Test feasibility and Multiple Imputation for participants who without data on on-Site visit. Data up to 9 months was used where 6 months data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

Secondary outcomes (11)
  1. Change From Baseline to 6 Months in Short Form-36 (SF-36) 10 Item Physical Function Domain (PF-10) Sub-score

    The Physical Function Domain (PF-10) of the SF-36 assesses an individual's perceived physical functioning and limitations in various activities. It consists of ten items that ask about a person's ability to perform different physical activities and tasks. Scores on the PF-10 range from 0 to 100 where 100 indicates no physical limitations. Missing data imputed using adjusted Bayesian MI methods. Data up to 9 month was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  2. Change From Baseline to 6 Months in Handgrip Strength Test

    Handgrip strength was a commonly used measure of upper body skeletal muscle function and had been widely used as a general indicator of frailty with predictive validity for both mortality and functional limitations. Participants were instructed to stand upright and with the dynamometer beside them but not against their body. Strength was measured three times for both hands. The highest value of all 3 attempts was kept for further analysis. Grip strength was measured in the dominant hand using a hydraulic grip strength dynamometer. Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  3. Change From Baseline to 6 Months in Appendicular Lean Body Mass (ALM) Based on Dual-energy X-ray Absorptiometry (DEXA) Measurements

    DEXA scans provided accurate measurements of body composition, recording fat and lean mass distribution throughout the entire body. Foundation of National Health Institute (FNIH) project report recommended ALM alone was used to measure gender-specific low muscle mass. Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  4. Rate of Response for Completing 400 MW Test After 6 Months

    A responder was defined as an improvement (increase) of 0.1 m/s or more in 400MW gait speed test compared to baseline. A non-responder was defined as a participant that was not a responder. Participants with a missing value at the visit and/or missing baseline value were considered as non-responders. Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  5. Change From Baseline to 6 Months in Muscle Strength Based on Knee Extension

    Isometric knee extension torque was measured with a knee extension dynamometer chair. The participants were positioned in an upright position, with straps to affix the hips to the chair and the ankle to a force or torque transducer at the knee angle of 90°. Lever arm length was recorded as the distance between the knee axis of rotation and the middle of the pad. Knee extension was measured using the maximum peak torque measurement Newton meter (Nm) for 60°/s, 90°/s and 180°/s for the tested leg (either right or left). The Knee extension torque was obtained either directly or by multiplying recorded peak force with the lever arm length. The assay with the highest torque output was taken for analyses. Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  6. Change From Baseline to 6 Months in Time for Five Chair Stands as Part of the Short Physical Performance Battery (SPPB) Assessment

    The SPPB was a series of tests designed to examine physical movements. The chair stands tests involved standing from a chair a number of times to test leg strength. Each performance measures were assigned a score ranging from 0 to 4, with 4 indicating the highest level of performance and 0 the inability to complete the test. The time to complete the task was recorded. The time required to perform five chair stands was scored as follows: ≥ 16.70 sec = 1; 13.70 to 16.69 sec = 2; 11.20 to 13.69 sec = 3; ≤ 11.19 = 4. A score of 0 was assigned to participants unable to perform the task. A summary score ranging from 0 (worst performers) to 12 (best performers) was calculated by adding sub scores from the chair stands test. Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  7. Change From Baseline to 6 Months in Distance in the 6-Minute Walk Test (6MWT)

    The 6MWT was a test for functional exercise capacity and involved measuring the distance a participant could cover within the allotted time of 6 minutes. Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  8. Change From Baseline to 6 Months in Pepper Assessment Tool for Disability (PAT-D) for Obese Participants

    The PAT-D was a disability questionnaire which asked respondents how much difficulty they had with a range of activities with functioning. PAT-D scores range from 1 (worst) to 5 (best). Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  9. Change From Baseline to 6 Months in SPPB Total Score

    The SPPB was a series of tests designed to examine physical movements. Results of the SPPB included total gait speed score, total balance test score, and total chair stand score. The first tests examined balance (without the assistance of a cane or walker) with the feet in three different orientations, the second test examined gait speed, and the third tests involved standing from a Chair a number of times to test leg strength. A score of 0 was assigned to participants unable to perform the task. A summary score ranging from 0 (worst performers) to 12 (best performers) was calculated by adding sub scores from the walking speed, chair stands and balance tests. Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  10. Change From Baseline to 6 Months in Sarcopenia Quality of Life (SarQoL) Auto-Evaluation Questionnaire

    The SarQoL was a sarcopenia-specific, self-administered, quality of life questionnaire designed for community-dwelling elderly study participants aged 65 years and older.

    The questionnaire contained 22 questions, which took approximately 10 minutes to complete. The questionnaire covered 7 domains: physical and mental health; locomotion; body composition; functionality; activities of daily living; leisure activities; and fears. Most questions are answered on a 4 point Likert scale. The total scoring of the SarQoL questionnaire ranges from 0 (worst imaginable health) to 100 (best imaginable health). A higher score reflected a higher quality of life. Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

  11. Change From Baseline to 6 Months in Stair Climb Power Test (SCPT)

    The SCPT measured the ability to ascend and descend stairs and tests lower body strength and balance and measures time (in seconds) taken to ascend and descend a flight of stairs (10 steps with a 20 cm step height; a handrail was recommended). Step heights should have been suitable (between 16 and 20 cm). Data up to month 9 was used where 6 month data were unavailable for participants enrolled during the COVID-19 pandemic.

    Measured: Baseline and 6 Months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Mar 2018
  2. Study start7 Feb 2017
  3. Primary completion26 Apr 2020
  4. Study completion26 Apr 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
233 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03452488
Sponsor's protocol ID
BIO101-CL03
Acronym
SARA-INT
Status last verified
Sep 2024
First submitted
13 Feb 2018
Last updated
1 Oct 2024
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing BIO101 in people with Sarcopenia and Gait Disorders in Old Age, run by Biophytis at 22 sites in 2 countries.

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 8 inclusion and 19 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: finished, as of the sponsor's last update on 1 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 22 sites in United States, Belgium. 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. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 1 Oct 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change From Baseline to 6 Months in Gait Speed for 400 Meter Walking (MW) Test (time frame: Baseline and 6 Months). 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 1 Oct 2024.

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