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Polycystic Ovary SyndromePhase 3NCT02635386

EQW, DAPA, EQW/DAPA, DAPA/MET ER and PHEN/TPM ER in Obese Women With PolycysticOvary Syndrome (PCOS)

A Phase 3 study testing Exenatide once weekly (EQW ), Dapagliflozin (DAPA) and EQW plus DAPA in people with Polycystic Ovary Syndrome and Obesity, run by Woman's at 1 site in United States.

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

This is a randomized, single-blind, parallel 5 treatment group 24-week trial designed to directly compare the therapeutic effects of exenatide once weekly (EQW), dapagliflozin (DAPA), EQW plus DAPA, combined DAPA/metformin extended release (XR) and the weight loss medication, phentermine/topiramate extended release… Read more about this study

Who is it for?
Ages 18 to 45 years, women onlyHealthy volunteers can take part
Conditions the study is for
Polycystic Ovary Syndrome, Obesity
What is being tested?
Exenatide once weekly (EQW ), Dapagliflozin (DAPA) and EQW plus DAPA
Could I receive a placebo?
No, everyone receives an active treatment
How many people
119 participants
Where
1 siteUnited States
Study dates
22 Mar 2016to 9 Oct 2020
Phase
Phase 3
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 18 to 45 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Non-diabetic women (18-45 years)
  • PCOS- NIH criteria hyperandrogenism and irregular menses
  • Obese class I, II, and III (BMI >30<45)
  • Willing to use effective contraception consistently during therapy which is defined as:
  • an intrauterine device, tubal sterilization, or male partner vasectomy, or
  • combination of two barrier methods with one being male condom.
  • Written consent for participation in the study

Who cannot join

  • Presence of significant systemic disease, heart problems including congestive heart failure, unstable angina or acute myocardial infarction, current infectious liver disease, acute stroke or transient ischemic attacks, history of pancreatitis, or diabetes mellitus (Type 1 or 2)
  • Any hepatic diseases in the past (infectious liver disease, viral hepatitis, toxic hepatic damage, jaundice of unknown etiology) or severe hepatic insufficiency and/or significant abnormal liver function tests defined as aspartate aminotransferase (AST) >3x upper limit of normal (ULN) and/or alanine aminotransferase (ALT) >3x ULN
  • Renal impairment (e.g., serum creatinine levels ≥1.4 mg/dL for women, or estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m2) or history of unstable or rapidly progressing renal disease or end stage renal disease. Patients with a history of nephrolithiasis are also excluded due to increased association with kidney stone formation.
  • Uncontrolled thyroid disease (documented normal TSH), Cushing's syndrome, congenital adrenal hyperplasia or hyperprolactinemia
  • Significantly elevated triglyceride levels (fasting triglyceride > 400 mg/dL)
  • Untreated or poorly controlled hypertension (sitting blood pressure > 160/95 mm Hg)
Show all 24Show fewer
  • Use of hormonal medications, lipid-lowering (statins, etc.), anti-obesity drugs or weight loss medications (prescription or OTC) and medications known to exacerbate glucose tolerance (such as isotretinoin, hormonal contraceptives, gonadotropin-releasing hormone agonists, glucocorticoids, anabolic steroids, C-19 progestins) stopped for at least 8 weeks. Use of anti-androgens that act peripherally to reduce hirsutism such as 5-alpha reductase inhibitors (finasteride, spironolactone, flutamide) stopped for at least 4 weeks
  • Prior history of a malignant disease requiring chemotherapy
  • Patients at risk for volume depletion due to co-existing conditions or concomitant medications, such as loop diuretics should have careful monitoring of their volume status
  • History of unexplained microscopic or gross hematuria, or microscopic hematuria at visit 1, confirmed by a follow-up sample at next scheduled visit.
  • Presence of hypersensitivity to dapagliflozin or other SGLT2 inhibitors (e.g. anaphylaxis, angioedema, exfoliative skin conditions
  • Known hypersensitivity or contraindications to use GLP1 receptor agonists (exenatide, liraglutide)
  • Use of metformin, thiazolidinediones, GLP-1 receptor agonists, dipeptidyl peptidase 4 (DPP-4) inhibitors, SGLT2 inhibitors stopped for at least 4 weeks.
  • Prior use of medication to treat diabetes except gestational diabetes
  • Eating disorders (anorexia, bulimia) or gastrointestinal disorders
  • Suspected pregnancy (documented negative serum pregnancy test), desiring pregnancy in next 6 months, breastfeeding, or known pregnancy in last 2 months
  • Active or prior history of substance abuse (smoke or tobacco use within past 3 years) or significant intake of alcohol
  • Having a history of bariatric surgery
  • Patient not willing to use two barrier method contraception during study period (unless sterilized or have an IUD)
  • Patients with glaucoma or history of increased intraocular pressure, or use of any medications to treat increased intraocular pressure
  • Debilitating psychiatric disorder such as psychosis or neurological condition that might confound outcome variables. Patients with a history of bipolar disorder or psychosis, greater than one lifetime, episode of major depression, current depression of moderate or greater severity (PHQ-9score of 10 or more), presence or history of suicidal behavior or ideation with some intent to act on it, or antidepressant use that has not been stable for at least 3 months will also be excluded.
  • Inability or refusal to comply with protocol
  • Current participation or participation in an experimental drug study in previous three months
  • -

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Woman's Hospital

    Baton Rouge, Louisiana, 70817

Other trials in United States

About this study

Official title: Comparison of Dapagliflozin (DAPA) and Once-weekly Exenatide (EQW), Co-administered or Alone, DAPA/ Glucophage (DAPA/MET ER) and Phentermine/Topiramate (PHEN/TPM) ER on Metabolic Profiles and Body Composition in Obese PCOS Women

This is a randomized, single-blind, parallel 5 treatment group 24-week trial designed to directly compare the therapeutic effects of exenatide once weekly (EQW), dapagliflozin (DAPA), EQW plus DAPA, combined DAPA/metformin extended release (XR) and the weight loss medication, phentermine/topiramate extended release (PHEN/TPM ER) on metabolic and endocrinological parameters in overweight/obese non-diabetic women with PCOS. In this study, we will examine the efficacy of these therapies on metabolic parameters, body weight and body composition, anthropometric measurements, and reproductive function in a well-defined group of pre-menopausal overweight/obese, non-diabetic women with PCOS, focusing on their relationship to insulin resistance and obesity. We hope to determine which treatment(s) addressing the multifaceted disturbances of individual subgroups emerge as the preferable therapy.

Read the detailed description

Polycystic ovary syndrome is a heterogeneous condition characterized by disordered reproductive and metabolic function which accounts for the myriad of clinical features including androgen excess, chronic anovulation, insulin resistance adiposity, and dyslipidemia. This syndrome is highly prevalent, affecting between 8 and 18% of the female population, depending on the diagnostic criteria used. Hyperandrogenism, ovarian dysfunction and metabolic abnormalities - the main determinants of PCOS - all appear to be involved in a synergistic way in the pathophysiology of PCOS. Women with PCOS are more likely to be obese: between 38 and 88% of women with PCOS are overweight or obese, although PCOS can also manifest in lean women. Obesity, particularly abdominal obesity, plays a central role in the development of PCOS, and exacerbates the reproductive and metabolic dysfunction. Rather than absolute body weight, it is the distribution of fat that is important with central (visceral) adiposity being a risk factor. Visceral adipose tissue is more metabolically active than subcutaneous fat and the amount of visceral fat correlates with insulin resistance and hyperinsulinemia. Weight gain is also often an important pathogenic factor, with PCOS usually becoming clinically manifest in women with a presumable genetic predisposition for PCOS who subsequently gain weight. Therefore, environmental (particularly dietary) factors are important. However, BMI is also influenced by genetic factors such as the fat mass and obesity-associated protein, and obesity is a highly heritable condition. Therefore, the weight gain responsible for the manifestation of PCOS in many women with this condition is itself influenced by genetic factors. Ethnicity, genetic background, personal and family history, degree of obesity must all be taken into account because they might aggravate or even trigger metabolic disturbances women with PCOS. Moreover, the incidence of glucose intolerance, dyslipidemia, gestational diabetes, and type 2 diabetes (DM2) is increased in women with PCOS at all weight levels and at a young age. PCOS may be a more important risk factor than ethnicity or race for glucose intolerance in young women. The exact factors responsible for this excess risk in women with PCOS have not been identified; family history of DM 2, obesity, insulin resistance, beta cell (ß-cell) secretory dysfunction, and hyperandrogenism are possible candidates. With better understanding of its pathophysiology, the metabolic consequences of the syndrome are now evident. Therefore, these patients need to be followed up even after their presenting complaint has been adequately resolved.

Lifestyle modification is a key component for the improvement of reproductive function for overweight, anovulatory women with PCOS. Even a modest weight loss 5% of total body weight can restore ovulation in overweight women with PCOS. Features of PCOS (e.g., hirsutism, testosterone levels, insulin resistance, menstrual cyclicity and ovulation) showed marked improvements, and PCOS frequently resolved after substantial weight loss induced by bariatric surgery. Recently a number of anti-diabetes medications have been approved which facilitate weight loss and improve the underlying insulin resistance. We reported that treatment with the glucagon like peptide -1 (GLP-1) agonist, exenatide for 24 weeks was superior to single agent metformin treatment in improving insulin action and reducing body weight and hyperandrogenism in obese women with PCOS. We further observed exenatide treatment significantly improved first-phase insulin responses to oral glucose administration. Since aberrant first-phase insulin secretion and impaired suppression of endogenous glucose production are major contributors to postprandial hyperglycemia and development of type 2 diabetes, the effects of exenatide once weekly [EQW (2 mg)] to target these defects, and normalize glucose excursions are likely to be clinically significant in obese patients with PCOS. Sodium/glucose cotransporter 2 (SGLT-2) inhibitors are the newest class of medications for diabetes management that have not been investigated for use in the women with PCOS. The SGLT2 inhibitor, dapagliflozin [DAPA (10 mg/day)] has an insulin-independent action, promotes weight loss, has a low incidence of hypoglycemia, and complements the action of other antidiabetic agents. The loss of glucose with attendant caloric loss contributes to weight loss; in addition, improvements in β cell function have been seen. Because the SGLT2 inhibitors have a distinct mechanism of action that is independent of insulin secretion, the efficacy of this class of drugs is not anticipated to decline in the presence of severe insulin resistance. The weight loss seen with SGLT2 inhibitors is similar to that seen with glucagon-like peptide 1 agonists, and may be more acceptable because they are oral agents. The resulting weight loss will further assist in decreasing insulin resistance, leading to increased glucose disposal thus contributing to an increased insulin secretion-insulin sensitivity (ISSI) index, the primary outcomes measure.

The non-diabetic female with PCOS offers a unique model to study the relationship between insulin resistance and adiposity. Women with PCOS demonstrate abnormal body composition characterized by a greater percent body fat, body fat mass, and increased ratio of fat to lean mass (F/L ratio). Studies using dual-energy X-ray absorptiometry (DEXA) methodology report a higher degree of metabolic dysfunction in patients with PCOS which appears be directly associated with their higher F/L ratio. Given that monotherapy and combined therapy with exenatide once weekly (EQW),and dapagliflozin (DAPA) along with DAPA/ metformin XR therapy are associated with weight loss introduces a confounder to the current study since it prevents distinguishing direct effects of the compounds on β-cell function vs. effects due to reduced adiposity. To control for loss of body mass and provide appropriate intervention in the remaining study arm we propose the use of a comparator weight loss drug alone, combination phentermine (PHEN)/topiramate (TPM) extended release (ER). To avoid the confounding relationship of body fat and insulin resistance, we will enroll only obese non-diabetic women with PCOS. All patients will receive diet and lifestyle counselling, including advice on exercise, according to usual clinical routine commencing during the lead-in period and continuing throughout the study We propose a randomized, single-blind, parallel 5 treatment group 24-week trial designed to directly compare the therapeutic effects of exenatide once weekly (EQW), dapagliflozin (DAPA), EQW plus DAPA, combined DAPA/metformin ER and the weight loss medication, phentermine/topiramate extended release (PHEN/TPM ER) on metabolic and endocrinological parameters in obese non-diabetic women with PCOS.

Being tested
Exenatide once weekly (EQW ), Dapagliflozin (DAPA), EQW plus DAPA, Dapagliflozin plus Glucophage (MET ER), Phentermine /Topiramate (PHEN/ TPM) ER
Keywords
PCOS, GLP1 agonists, SGLT2 inhibitors
Medical subject headings
Polycystic Ovary Syndrome, Obesity

What participants receive

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

  • Exenatide once weekly (EQW )Drug

    Also called • Bydureon, • Long acting glucagon like peptide 1 (GLP1) agonist

    2 mg SC injection every 7 days

  • Dapagliflozin (DAPA)Drug

    Also called • Farxiga, • SGLT2 inhibitor

    One pill (10 mg) by mouth daily (QD) in am

  • EQW plus DAPADrug

    Also called Bydureon plus Farxiga, Long acting GLP1 agonist plus SGLT2 inhibitor

    2 mg SC injection every 7 days One pill (10 mg) by mouth QD in am

  • Dapagliflozin plus Glucophage (MET ER)Drug

    Also called Xigduo, •Combination SGLT2 inhibitor and metformin ER

    DAPA/MET ER-5 mg /1000 mg - 1 pill by mouth in am with food for 4 weeks DAPA/MET ER-10 mg /2000 mg - 2 pills in am by mouth with food -final dose

  • Phentermine /Topiramate (PHEN/ TPM) ERDrug

    Also called Qsymia

    PHEN 3.75/TPM ER 23mg - 1 pill by mouth once daily in am for 2 weeks. After 2 weeks, PHEN 7.5mg/TPM ER 46mg- 1 pill by mouth once daily in am

Study groups in NCT02635386
Study groupRoleWhat they receive
Exenatide once weekly (EQW )ExperimentalEQW- 2 mg subcutaneous (SC) injection once every seven days for 24 weeks
Receives: Drug: Exenatide once weekly (EQW )
Dapagliflozin (DAPA)ExperimentalDAPA-10 mg oral pill once daily in am for 24 weeks
Receives: Drug: Dapagliflozin (DAPA)
EQW plus DAPAExperimentalEQW- 2 mg SC injection once every seven days for 24 weeks DAPA-10 mg oral pill once daily in am daily for 24 weeks
Receives: Drug: EQW plus DAPA
Dapagliflozin plus Glucophage (MET ER)ExperimentalCombination DAPA / MET ER-10 mg /2000 mg oral pill daily with food for 24 weeks
Receives: Drug: Dapagliflozin plus Glucophage (MET ER)
Phentermine /Topiramate (PHEN/ TPM) ERActive comparatorCombination Phentermine /Topiramate ER -7.5 mg/46mg pill once daily in am for 24 weeks
Receives: Drug: Phentermine /Topiramate (PHEN/ TPM) ER

What is being measured

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

  1. Oral Disposition (Insulin Sensitivity-insulin Secretion) Index

    An estimation of β-cell compensatory function, the insulin secretion-sensitivity index (IS-SI) will be derived by applying the concept of the oral disposition index to measurements obtained during the 2-h OGTT and calculated as the index of insulin secretion factored by insulin sensitivity (ΔINS/ΔPG 30 x Matsuda SIOGTT) from the OGTT. A higher score shows improved pancreatic insulin responsiveness relative to resistance.

    Measured: 24 weeks of treatment

Secondary outcomes (22)
  1. Absolute Body Weight

    Treatment effect on body weight at 24 weeks of treatment

    Measured: 24 weeks of treatment

  2. Body Mass Index (BMI)

    Treatment efficacy in reducing body mass at 24 weeks of treatment

    Measured: 24 weeks of treatment

  3. Change in Percent Body Weight

    Treatment effect on change in percent body weight from baseline

    Measured: Change from baseline (time 0) to study end (24 weeks)

  4. Central Adiposity (Waist Circumference)

    Treatment effect on loss of central adiposity after 24 weeks

    Measured: 24 weeks of treatment

  5. Waist-to-Hip Ratio (WHR)

    Treatment impact on central adiposity after 24 weeks

    Measured: 24 weeks of treatment

  6. Waist-to-Height Ratio (WHtR)

    Treatment impact on WHtR which is a measure of central adiposity

    Measured: 24 weeks of treatment

  7. Total Fat Mass (kg) Evaluated by DEXA

    Treatment impact on total fat mass by DEXA

    Measured: 24 weeks of treatment

  8. Total Body Fat (%) by DEXA

    Treatment impact on percent total body fat by DEXA

    Measured: 24 weeks of treatment

  9. Android-Gynoid Ratio (AGR) as Determined by DEXA

    treatment impact on measure of central adiposity as determined by android/gynoid ratio

    Measured: 24 weeks of treatment

  10. Trunk/Leg Fat Ratio by DEXA

    Treatment impact on trunk/limb ratio (measure of central adiposity) by DEXA

    Measured: 24 weeks of treatment

  11. Fasting Blood Glucose

    Treatment impact on fasting concentration of glucose in the blood

    Measured: 24 weeks of treatment

  12. OGTT Mean Blood Glucose (MBG)

    Treatment effect on MBG measured during the oral glucose tolerance test

    Measured: 24 weeks of treatment

  13. Fasting Insulin Sensitivity (HOMA-IR)

    Treatment effect on the ratio HOMA-IR which is insulin resistance measure derived from fasting blood glucose and insulin and is calculated by insulin (mU/ml)*glucose (mmol/L)/22,5. The higher thenumber the more insulin resistant.

    Measured: 24 weeks of treatment

  14. Matsuda Sensitivity Index Derived From the OGTT(SI OGTT)

    The SI IOGTT is a measure of peripheral insulin sensitivity derived from the values of Insulin (microunits per milliliter) and Glucose (milligrams per deciliter) obtained from the OGTT and the corresponding fasting values. SI (OGTT) = 10,000/ [(G fasting x I fasting) x (G OGTTmean x I OGTTmean)], where fasting glucose and insulin data are taken from time 0 of the OGTT and mean data represent the average glucose and insulin values obtained during the entire OGTT. The square root is used to correct for nonlinear distribution of insulin, and 10,000 is a scaling factor in the equation. The higher value, the more sensitive to insulin.

    Measured: 24 weeks of treatment

  15. Corrected First Phase Insulin Secretion (IGI/HOMA-IR)

    Treatment effect on insulin secretion from 0 to 30 minutes after glucose load corrected for by fasting insulin sensitivity. A higher score shows improved first phase insulin secretion in response to glucose

    Measured: 24 weeks of treatment

  16. Total Cholesterol Levels

    Treatment effect on blood concentrations of total cholesterol

    Measured: 24 weeks of treatment

  17. Triglyceride (TRG) Levels

    Treatment effect on blood concentrations of triglycerides

    Measured: 24 weeks of treatment

  18. Total Testosterone Concentrations

    Treatment effect on blood concentrations of total testosterone

    Measured: 24 weeks of treatment

  19. Dehydroepiandrosterone Sulfate (DHEA-S) Levels

    Treatment effect on blood concentrations of DHEA-S

    Measured: 24 weeks of treatment

  20. Free Androgen Index (FAI)

    Treatment effect on FAI calculated from total testosterone divided by sex hormone binding globulin (SHBG) levels. A higher score indicates a worse outcome.

    Measured: 24 weeks of treatment

  21. Systolic Blood Pressure (SBP)

    Treatment effect on SBP after 24 weeks of treatment

    Measured: 24 weeks treatment

  22. Diastolic Blood Pressure (DBP)

    Treatment effect on DBP after 24 weeks

    Measured: 24 weeks of treatment

Timeline

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

  1. First posted18 Dec 2015 (estimated)
  2. Study start22 Mar 2016
  3. Primary completion22 Jul 2020
  4. Study completion9 Oct 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 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
119 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02635386
Sponsor's protocol ID
RP15-008
Other IDs
AZ ESR-14-10725
Status last verified
Jan 2021
First submitted
15 Dec 2015
Last updated
29 Jan 2021
Data monitoring committee
Yes
Individual data sharing
No: Individual data will only be shared with participant

Publications

  • Elkind-Hirsch KE, Chappell N, Seidemann E, Storment J, Bellanger D. Exenatide, Dapagliflozin, or Phentermine/Topiramate Differentially Affect Metabolic Profiles in Polycystic Ovary Syndrome. J Clin Endocrinol Metab. 2021 Sep 27;106(10):3019-3033. doi: 10.1210/clinem/dgab408.

    PubMed 34097062

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Exenatide once weekly (EQW ), Dapagliflozin (DAPA) and EQW plus DAPA in people with Polycystic Ovary Syndrome and Obesity, run by Woman's at 1 site 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 7 inclusion and 24 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 29 Jan 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site 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.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

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 29 Jan 2021). 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?

Oral Disposition (Insulin Sensitivity-insulin Secretion) Index (time frame: 24 weeks of treatment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02635386, which also lists 1 linked publication.

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 29 Jan 2021.

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