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Trial · Interventional

CompletedPhase 3Results postedRegistry data

A Phase 3 Study to Evaluate the Efficacy and Safety of Relugolix (TAK-385) 40 mg Compared With Leuprorelin in the Treatment of Uterine Fibroids

NCTNCT02655237 (opens ClinicalTrials.gov in a new tab)Other idTAK-385/CCT-002Other idU1111-1178-0989Other idJapicCTI-163128

Overview

Status
Completed
Phase
Phase 3
Enrollment
281 participants (actual)
Sponsor
Takeda · Industry
Design
Randomized · Quadruple masking
Countries
1 country

Japan

Start
5 Mar 2016
Primary completion
17 May 2017
Completion
25 Sept 2017
First posted
13 Jan 2016 (estimated)
Last update posted
22 Mar 2019
Conditions
Uterine Fibroids

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
201620172018
  1. Ph 3

    A Phase 3 Study to Evaluate the Efficacy and Safety of Relugolix (TAK-385) 40 mg Compared With Leuprorelin in the Treatment of Uterine Fibroids

    NCT02655237

    5 Mar 2016 to 25 Sept 2017

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The purpose of this study is to evaluate the efficacy of Relugolix (TAK-385) 40 mg administered orally once daily for 12 weeks, compared with leuprorelin injection (once every 4 weeks, 1.88 mg or 3.75 mg subcutaneously \[SC\]/time) in patients with uterine fibroids.

Interventions

  • RelugolixDrug
  • Relugolix PlaceboDrug
  • LeuprorelinDrug
  • Leuprorelin PlaceboDrug

Arms2

  • Experimental

    Relugolix 40 mg

    Relugolix placebo matching tablets, orally, once daily along with leuprorelin acetate placebo matching injection, SC, once in 4 weeks for 3 to 6 weeks in run-in period followed by relugolix 40 mg, tablets, orally, once daily and leuprorelin acetate placebo matching injection, SC, once in 4 weeks for 24 weeks in treatment period.

  • Active comparator

    Leuprorelin 1.88 mg or 3.75 mg

    Relugolix placebo matching tablets, orally, once daily along with leuprorelin acetate placebo matching injection, SC, once in 4 weeks for 3 to 6 weeks in run-in period followed by leuprorelin acetate 1.88 mg or 3.75 mg, injection, SC, once in 4 weeks and relugolix placebo matching tablets, orally, once daily for 24 weeks in treatment period.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Percentage of Participants With Total PBAC Score of <10 From Week 6 to 12

    Time frame · Week 6 to 12

    Registry description

    PBAC score was used to measure volume of menstrual blood loss. Participants used sanitary products designated by sponsor and recorded the numbers of tampons or towels used, clots and flooding in patient diary. Three diagrams used which represented a lightly, moderately stained or completely saturated pad/tampon. Following scores assigned: 1) 1, 5, or 20 points for each pad; 2) 1, 5, or 10 points for each tampon; 3) 1 or 5 points for each blood clot of \<1 cm/=1 cm/\>1 in longest diameter; 4) 5 points for each episode of flooding. The total PBAC score (sum of points) ranges from 0 to \>500.

Secondary outcomes(16)
  1. Percentage of Participants With Total PBAC Score of <10 From Week 2 to 6

    Time frame · Week 2 to 6

    Registry description

    PBAC score was used to measure volume of menstrual blood loss. Participants used sanitary products designated by sponsor and recorded the numbers of tampons or towels used, clots and flooding in patient diary. Three diagrams used which represented a lightly, moderately stained or completely saturated pad/tampon. Following scores assigned: 1) 1, 5, or 20 points for each pad; 2) 1, 5, or 10 points for each tampon; 3) 1 or 5 points for each blood clot of \<1 cm/=1 cm/\>1 in longest diameter; 4) 5 points for each episode of flooding. The total PBAC score (sum of points) ranges from 0 to \>500.

  2. Percentage of Participants With Total PBAC Score of <10 From Week 18 to 24

    Time frame · Week 18 to 24

    Registry description

    PBAC score was used to measure volume of menstrual blood loss. Participants used sanitary products designated by sponsor and recorded the numbers of tampons or towels used, clots and flooding in patient diary. Three diagrams used which represented a lightly, moderately stained or completely saturated pad/tampon. Following scores assigned: 1) 1, 5, or 20 points for each pad; 2) 1, 5, or 10 points for each tampon; 3) 1 or 5 points for each blood clot of \<1 cm/=1 cm/\>1 in longest diameter; 4) 5 points for each episode of flooding. The total PBAC score (sum of points) ranges from 0 to \>500.

  3. Percentage of Participants With Total PBAC Score of <10 for 6 Weeks Before the Final Dose of Study Drug

    Time frame · For 6 weeks before the final dose of study drug (up to Week 24)

    Registry description

    PBAC score was used to measure volume of menstrual blood loss. Participants used sanitary products designated by sponsor and recorded the numbers of tampons or towels used, clots and flooding in patient diary. Three diagrams used which represented a lightly, moderately stained or completely saturated pad/tampon. Following scores assigned: 1) 1, 5, or 20 points for each pad; 2) 1, 5, or 10 points for each tampon; 3) 1 or 5 points for each blood clot of \<1 cm/=1 cm/\>1 in longest diameter; 4) 5 points for each episode of flooding. The total PBAC score (sum of points) ranges from 0 to \>500.

  4. Percent Change From Baseline in Myoma Volumes at Weeks 2, 4, 8, 12 and 24

    Time frame · Baseline, Weeks 2, 4, 8, 12 and 24

    Registry description

    A transvaginal ultrasound was performed to determine myoma volumes. Only the largest myoma among those measurable at visit 1 was measured throughout the study. On the assumption that the myoma was spheroids, the myoma volumes were calculated using 3 diameters (D1, D2, and D3). D1: the longest diameter of the myoma; D2: the longest diameter of the myoma which was perpendicular to D1; D3: the diameter of the myoma which crossed the intersection of D1 and D2 (intersection "Z") and was perpendicular to D1/D2 plane. The formula used for calculation is Myoma volume= D1\*D2\*D3\*π/6.

  5. Percent Change From Baseline in Uterine Volumes at Weeks 2, 4, 8, 12 and 24

    Time frame · Baseline, Weeks 2, 4, 8, 12 and 24

    Registry description

    A transvaginal ultrasound was performed for determination of uterine volumes. On the assumption that the uterus was spheroids, the uterine volumes were calculated using 3 diameters (D1, D2, and D3) measured as shown below: D1: the longest diameter of the uterus (unit of length: cm); D2: the longest diameter of the uterus which was perpendicular to D1 (unit of length: cm); D3: the diameter of the uterus which crossed the intersection of D1 and D2 (intersection "Z") and was perpendicular to D1/D2 plane (unit of length: cm). The formula used for calculation is Uterine volume=D1\*D2\*D3\*π/6.

  6. Change From Baseline in Hemoglobin at Weeks 4, 8, 12, 16, 20, 24 and Follow up

    Time frame · Baseline, Weeks 4, 8, 12, 16, 20, 24 and Follow up (up to Week 28)

    Registry description

    Anemia-related measurements consisted of hemoglobin, which were determined at the central laboratory.

  7. Numerical Rating Scale (NRS) Score

    Time frame · From Week 6 to 12, from Week 2 to 6, from Week 18 to 24, and for 6 weeks before the final dose (up to Week 24)

    Registry description

    Pain symptoms were evaluated using the NRS score. NRS score is a self-reported instrument assessing pain from 0 to 10. Higher scores reflect greater level of pain.

  8. Change From Baseline in Uterine Fibroid Symptom and Quality of Life (UFS-QOL)- Symptom Severity Score at Weeks 4, 8, 12, 16, 20, 24 and Follow-up

    Time frame · Baseline, Weeks 4, 8, 12, 16, 20, 24 and Follow-up (up to Week 28)

    Registry description

    UFS-QOL was a 37-item self-reporting tool for evaluating QOL in participants with uterine fibroid. It includes eight symptom-related questions and 29 HRQL questions across six subscales (concern, activities, energy/mood, control, self-consciousness, sexual function). The total symptom severity score is ranging from 0 to 100. The higher scores indicate greater severity.

  9. Change From Baseline in Uterine Fibroid Symptom and Quality of Life (UFS-QOL)- HRQL Total Scores at Weeks 4, 8, 12, 16, 20, 24 and Follow-up

    Time frame · Baseline, Weeks 4, 8, 12, 16, 20, 24 and Follow-up (up to Week 28)

    Registry description

    UFS-QOL was a 37-item self-reporting tool for evaluating QOL in participants with uterine fibroid. It includes eight symptom-related questions and 29 HRQL questions across six subscales (concern, activities, energy/mood, control, self-consciousness, sexual function). The total HRQL score is ranging from 0 to 100. The higher scores indicate better QOL.

  10. Number of Participants Who Had One or More Treatment Emergent Adverse Event (TEAE)

    Time frame · Up to Week 28

    Registry description

    An Adverse Event (AE) is defined as any untoward medical occurrence in a clinical investigation participant administered a drug; it does not necessarily have to have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (eg, a clinically significant abnormal laboratory finding), symptom, or disease temporally associated with the use of a drug, whether or not it is considered related to the drug. A treatment-emergent adverse event (TEAE) is defined as an adverse event with an onset that occurs after receiving study drug.

  11. Number of Participants With Markedly Abnormal Values of Vital Signs

    Time frame · Up to Week 28

    Registry description

    Vital signs included sitting blood pressure (after the participant has rested for at least 5 minutes), body temperature (oral or tympanic measurement) (degree Celsius \[°C\]) and pulse (beats per minute \[bpm\]) is reported.

  12. Number of Participants With TEAE Related to Weight

    Time frame · Up to Week 28

    Registry description

    Number of participants with TEAEs of which threshold was 5% or above in either treatment group related to weight was reported.

  13. Number of Participants With TEAE Related to Standard 12-Lead ECGs

    Time frame · Up to Week 28

    Registry description

    Number of participants with TEAEs of which threshold was 5% or above in either treatment group related to ECG was reported.

  14. Number of Participants With Markedly Abnormal Values of Laboratory Test

    Time frame · Up to Week 28

    Registry description

    Number of participants with any markedly abnormal values in laboratory tests collected throughout study is reported. WBC = White blood cells, AST = Aspartate Aminotransferase, ALT = Alanine Aminotransferase, GGT = gamma-glutamyl transferase, ULN = upper limit of normal or upper reference limit.

  15. Number of Participants With TEAE (Bone Density Decreased) Related to Bone Mineral Density

    Time frame · Up to Week 28

    Registry description

    Number of participants with TEAEs of which threshold was 5% or above in either treatment group related to bone mineral density was reported.

  16. Number of Participants With TEAE Related to Biochemical Bone Metabolism Markers

    Time frame · Up to Week 28

    Registry description

    Number of participants with TEAEs of which threshold was 5% or above in either treatment group related to biochemical bone metabolism markers was reported.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeNumber· Week 6 to 12

Percentage of Participants With Total PBAC Score of <10 From Week 6 to 12

GroupValue (percentage of participants)
Relugolix 40 mg82.2
Leuprorelin 1.88 mg or 3.75 mg83.1
Secondary and other outcome results(7)
Secondary outcomeNumber· Week 2 to 6

Percentage of Participants With Total PBAC Score of <10 From Week 2 to 6

GroupValue (percentage of participants)
Relugolix 40 mg64.2
Leuprorelin 1.88 mg or 3.75 mg31.7
Secondary outcomeNumber· Week 18 to 24

Percentage of Participants With Total PBAC Score of <10 From Week 18 to 24

GroupValue (percentage of participants)
Relugolix 40 mg84.1
Leuprorelin 1.88 mg or 3.75 mg94.7
Secondary outcomeNumber· For 6 weeks before the final dose of study drug (up to Week 24)

Percentage of Participants With Total PBAC Score of <10 for 6 Weeks Before the Final Dose of Study Drug

GroupValue (percentage of participants)
Relugolix 40 mg79.0
Leuprorelin 1.88 mg or 3.75 mg92.3
Secondary outcomeMean· Baseline, Weeks 2, 4, 8, 12 and 24

Percent Change From Baseline in Myoma Volumes at Weeks 2, 4, 8, 12 and 24

GroupValue (cm^3)Spread
Relugolix 40 mg-18.7431.849
Leuprorelin 1.88 mg or 3.75 mg-6.6833.377
Secondary outcomeMean· Baseline, Weeks 2, 4, 8, 12 and 24

Percent Change From Baseline in Uterine Volumes at Weeks 2, 4, 8, 12 and 24

GroupValue (cm^3)Spread
Relugolix 40 mg-22.0517.870
Leuprorelin 1.88 mg or 3.75 mg-6.9027.984
Secondary outcomeMean· Baseline, Weeks 4, 8, 12, 16, 20, 24 and Follow up (up to Week 28)

Change From Baseline in Hemoglobin at Weeks 4, 8, 12, 16, 20, 24 and Follow up

GroupValue (g/dL)Spread
Relugolix 40 mg0.790.763
Leuprorelin 1.88 mg or 3.75 mg0.600.789
Secondary outcomeMean· From Week 6 to 12, from Week 2 to 6, from Week 18 to 24, and for 6 weeks before the final dose (up to Week 24)

Numerical Rating Scale (NRS) Score

GroupValue (score on a scale)Spread
Relugolix 40 mg0.210.500
Leuprorelin 1.88 mg or 3.75 mg0.140.363

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Relugolix 40 mgRelugolix placebo matching tablets, orally, once daily along with leuprorelin acetate placebo matching injection, subcutaneously (SC), once in 4 weeks for 3 to 6 weeks in run-in period followed by relugolix 40 mg, tablets, orally, once daily and leuprorelin acetate placebo matching injection, SC, once in 4 weeks for 24 weeks in treatment period.0 / 1380 / 138123 / 138
Leuprorelin 1.88 mg or 3.75 mgRelugolix placebo matching tablets, orally, once daily along with leuprorelin acetate placebo matching injection, subcutaneously (SC), once in 4 weeks for 3 to 6 weeks in run-in period followed by leuprorelin acetate 1.88 mg or 3.75 mg, injection, SC, once in 4 weeks and relugolix placebo matching tablets, orally, once daily for 24 weeks in treatment period.0 / 1422 / 142134 / 142

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

Studies with results

1 study on this page

Indexing hint: Observational study · 2019

9 results

Oral Gonadotropin-Releasing Hormone Antagonist Relugolix Compared With Leuprorelin Injections for Uterine Leiomyomas: A Randomized Controlled Trial.

Osuga et al. 2019Obstetrics and gynecologycited by 70

PMID 30741797DOI 10.1097/aog.0000000000003141PUB-30741797

Full text at the publisher9 results

Eligibility

Who could join, as posted.

Sex
Female
Age
from 20 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: Inclusion Criteria for Entering the Screening (at VISIT 1) 1. In the opinion of the investigator or subinvestigator, the participant is capable of understanding and complying with protocol requirements. 2. The participant signs and dates a written, informed consent form prior to the initiation of any study procedures. 3. Prior to VISIT 1, the participant has a diagnosis of uterine fibroids confirmed by transvaginal ultrasound, abdominal ultrasound, magnetic resonance imaging (MRI), computed tomography (CT), or laparoscopy, and has never received any surgical treatment for the myoma (measurable noncalcified myoma with the longest diameter of ≥ 3 cm). 4. The participant is a premenopausal Japanese woman. 5. The participant is aged 20 years or older on the day of signing and dating the informed consent form. 6. The participant has 1 or more measurable noncalcified myomas with the longest diameter of ≥ 3 cm confirmed by transvaginal ultrasound. 7. The participant has experienced 1 or more regular menstrual cycles (25 to 38 days) immediately prior to VISIT 1 and that should include menstrual bleeding for at least 3 consecutive days. 8. The participant who is sexually active with a nonsterilized male partner agrees to use routinely adequate contraception from signing of informed consent throughout the study. Inclusion Criteria for Entering the Run-in (at VISIT 2) 9. The participant has experienced regular menstrual cycles (25 to 38 days) immediately prior to VISIT 2 that should include menstrual bleeding of at least 3 consecutive days (at least 2 regular menstruation cycles to be confirmed by Inclusion criteria #7 and #9). Inclusion Criteria for Entering the Treatment (at VISIT 3) 10. The participant has 1 or more measurable noncalcified myomas, with a longest diameter of ≥ 3 cm confirmed by transvaginal ultrasound (the same myoma should be measured as in Inclusion criterion #6). 11. The participant has a diagnosis of menorrhagia with a total Pictorial Blood loss Assessment Chart (PBAC) score of ≥ 120 in 1 menstrual cycle just before VISIT 3. 12. The participant has experienced regular menstrual cycles (25 to 38 days) after VISIT 1 that should include menstrual bleeding for at least 3 consecutive days (at least 3 regular menstruation cycles to be confirmed by Inclusion criteria #7, #9 and #12). Exclusion Criteria: 1. The participant has received any investigational compound within 24 weeks prior to the start of the administration of the study medication for the Run-in (VISIT 2). 2. The participant has received relugolix (including placebo) in a previous clinical study. 3. The participant is an immediate family member, study site employee, or is in a dependent relationship with a study site employee who is involved in conduct of this study (eg, spouse, parent, child, sibling) or may consent under duress. 4. The participant has a previous or current history of blood disorders (eg, thalassemia, sickle cells anemia, folic-acid deficiency, and coagulopathy), excluding (latent) iron-deficiency anemia. 5. The participant has a known history of severe hypersensitivity or severe allergy to sanitary goods. 6. The participant has lower abdominal pain due to irritable bowel syndrome or severe interstitial cystitis. 7. The participant has a current history of thyroid gland disorder with irregular menstruation, or has a potential for irregular menstruation due to thyroid gland disorder, as determined by the investigator or subinvestigator. 8. The participant has a previous or current history of pelvic inflammatory disease within 8 weeks prior to VISIT 1. 9. The participant has a positive Pap smear test result obtained within 1 year prior to VISIT 1 (if there are no previous test results, those who were judged positive in the test conducted before VISIT 2). 10. The participant has a history of panhysterectomy or bilateral oophorectomy. 11. The participant has had markedly abnormal uterine bleeding or anovulatory bleeding, as determined by the investigator or subinvestigator. 12. The participant has a malignant tumor or a history of a malignant tumor within 5 years prior to VISIT 1. 13. The participant has been treated with any of the following drugs (excluding drugs for external use and dietary supplements) within 4 weeks prior to VISIT 2: anti-coagulant drugs, anti-platelet drugs, tranexamic acid, selective estrogen receptor modulators (SERMs), activated vitamin D preparations, other vitamin D preparations, calcitonin, ipriflavone, steroid hormones, vitamin K preparations, teriparatide, or denosumab. 14. The participant has been treated with any of the following drugs within 8 weeks prior to VISIT 2: oral contraceptive or sex hormone preparations (norethindrone, norethisterone, medroxyprogesterone, estrogen, or other progestins), and within 16 weeks prior to VISIT 2: gonadotropin-releasing hormone (GnRH) analogues, dienogest, danazol, or aromatase inhibitors (for 1- and 3-month sustained-release preparations, within 20 and 28 weeks prior to VISIT 2, respectively). 15. The participant has been treated with a bisphosphonate preparation within 24 weeks prior to VISIT 2. 16. The participant has a previous or current history of hypersensitivity or allergies to leuprorelin, synthetic GnRH, GnRH agonists or GnRH antagonists, or has a previous or current history of severe hypersensitivity or severe allergy to other drugs. 17. The participant has nondiagnosable abnormal genital bleeding. 18. Female participant who is pregnant, lactating, or intending to become pregnant or to donate ova prior to the signing of informed consent, during the study period, or within 1 month after the end of the study. 19. The participant has a previous or current history of osteoporosis, osteopenia, or other metabolic bone diseases. 20. The participant has clinically significant cardiovascular disease (eg, myocardial infarction or unstable angina pectoris within 24 weeks prior to VISIT 1) or uncontrollable hypertension (eg, resting systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 110 mmHg at Screening and Run-in). 21. The participant is inappropriate for participation in this study based on standard 12-lead electrocardiogram (ECG) findings, as determined by the investigator or subinvestigator. 22. The participant has active liver disease or jaundice, or with alanine aminotransferase (ALT), aspartate aminotransferase (AST), or bilirubin (total bilirubin) \> 1.5 times the upper limit of normal (ULN) in the clinical laboratory tests at VISITs 1 and 2. 23. The participant has previous or current history of diseases considered to be inappropriate for participation in this study, including severe hepatic impairment, jaundice, renal impairment, cardiovascular disease, endocrine system disease, metabolic disorder, pulmonary disease, gastrointestinal disease, neurological disease, urological disease, immune disease, or mental disorder (especially depression-like symptoms) or suicide attempt resulting from a mental disorder. 24. The participant has a previous or current history of drug abuse (defined as any illicit drug use) or alcohol abuse. 25. The participant is inappropriate for participation in this study for other reasons, as determined by the investigator or subinvestigator.

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