PoC Study of OBE022 in Threatened Preterm Labour (PROLONG)
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03369262 |
|
Recruitment Status :
Active, not recruiting
First Posted : December 11, 2017
Last Update Posted : June 7, 2021
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
This is a proof-of-concept study in 2 parts.
In Part A, patients will receive OBE022 open-label in order to assess the safety and pharmacokinetics in pregnant women with spontaneous preterm labour with a gestational age between 28 0/7 and 33 6/7 weeks.
Part B has a double-blind, randomised, placebo controlled, parallel group and multicentre design and will assess the efficacy, safety and pharmacokinetics in pregnant women with threatened spontaneous preterm labour with a gestational age between 24 0/7 and 33 6/7 weeks.
All patients in part A and part B must receive atosiban infusion for 48 hours as standard of care treatment. Patients from Part A will receive OBE022 open label. Patients from Part B will be randomised to receive OBE022 or matching placebo. IMP treatment duration will be up to 7 days. IMP treatment will be stopped in case of delivery prior to Day 7.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Preterm Labor | Drug: OBE022 Drug: Placebos Drug: Atosiban | Phase 2 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 115 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Intervention Model Description: | A phase 2a, double-blind, parallel group, randomised, placebo controlled, added-on to atosiban. |
| Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
| Masking Description: | Matching placebo. |
| Primary Purpose: | Treatment |
| Official Title: | A Phase 2a, Double-blind, Parallel Group, Randomised, Placebo Controlled, Proof of Concept Study to Assess the Efficacy, Safety and Pharmacokinetics of OBE022 added-on to Atosiban, After Oral Administration in Pregnant Women With Threatened Spontaneous Preterm Labour |
| Actual Study Start Date : | January 10, 2018 |
| Actual Primary Completion Date : | July 8, 2020 |
| Estimated Study Completion Date : | August 2022 |
| Arm | Intervention/treatment |
|---|---|
|
Experimental: Active
OBE022 plus atosiban: OBE022 will be given orally from Day 1 to Day 7. OBE022 treatment will be initiated ideally simultaneously or at a maximum within 24 h after atosiban start.
Atosiban will be administered over 48h as per label. |
Drug: OBE022
Oral Drug: Atosiban I.V. |
|
Active Comparator: Placebo
OBE022 matching placebo plus atosiban: OBE022 matching placebo administration will follow the same regimen as the active group. Atosiban will be administered over 48h as per label. |
Drug: Placebos
Oral Drug: Atosiban I.V. |
- Incidence of delivery within 2 days (48 h) from start of IMP administration [ Time Frame: 48 hours ]
- Incidence of delivery within 7 days (168 h) from start of IMP administration [ Time Frame: 168 hours ]
- Incidence of delivery before 37 weeks of GA [ Time Frame: Up to 13 weeks from start of IMP administration ]
- Time to delivery measured from start of IMP administration [ Time Frame: Up to 17 weeks from start of IMP administration ]
- Maternal incidence of AEs from Day 1 until 28 days after birth. [ Time Frame: 28 days after birth ]
- Maternal incidence of TEAEs from Day 1 until 28 days after birth. [ Time Frame: 28 days after birth ]
- Maternal incidence of clinically significant changes in laboratory safety tests, from Day 1 until 28 days after birth. [ Time Frame: 28 days after birth ]
- Maternal incidence of clinically significant changes in vital signs, from Day 1 until 28 days after birth. [ Time Frame: 28 days after birth ]
- Incidence of AEs indicating fœtal distress such as growth retardation and/or changes in fœtal heart rate monitoring and/or amniotic fluid index (AFI) from Day 1 to Day 7 and Day 14 (or earlier if birth). [ Time Frame: Up to 14 days after start of IMP administration ]
- In Part A only: Incidence of fœtal adverse events in relation with the cardiovascular function assessed by Doppler ultrasound on Day 1 to 3 and Day 7 from IMP start. [ Time Frame: Up to 7 days after start of IMP administration ]
- Incidence of infants experiencing adverse events from birth until 28 days after birth. [ Time Frame: Up to 28 days after birth ]
- Incidence of infants experiencing clinical significant changes in vital signs from birth until 28 days after birth. [ Time Frame: Up to 28 days after birth ]
- Apgar score. [ Time Frame: At birth, at 1 minute and 5 minute ]The score is a rapid method for assessing a neonate immediately after birth. Elements of the Apgar score include color, heart rate, reflexes, muscle tone, and respiration, each weighted evenly and assigned a value of 0, 1, or 2. The components are then added together to give a total score (0 to 10) that is recorded at 1 and 5 minutes after birth.
- Weight. [ Time Frame: At birth and 28 days after birth. ]
- Head circumference. [ Time Frame: At birth and 28 days after birth. ]
- Incidence of infants experiencing prematurity-related events [ Time Frame: At birth. ]
- Incidence of duration of hospitalization and or re-admission to hospital. [ Time Frame: Up to 28 days after birth. ]
- Incidence of infants with one or more Ages and Stages Questionnaire® domain score(s) below the cut-off score at 6 months, 12 months and 24 months of age, adjusted for gestational age at birth. [ Time Frame: Up to 24 months ]The Ages and Stages Questionnaire (ASQ) is a parent-completed questionnaire designed to be used as a general developmental screening tool. The ASQ-3 covers five areas of child development that includes: personal social, gross motor, fine motor, problem solving, and communication. Parents complete the questionnaire independent of professionals, indicating for each item "yes" if child performs the item, "sometimes" indicating an occasional or emerging skill, or "not yet" indicating that the child does not yet perform the behavior
- Plasma concentration of OBE022/OBE002 at Day 1, Day 2, Day 3 and Day 7. [ Time Frame: Up to 7 days after start of IMP administration ]
- Pharmacokinetic parameters of OBE022/OBE002 at Day 7 [ Time Frame: Day 7 ]Area under the curve (AUC)
- Pharmacokinetic parameters of OBE022/OBE002 at Day 7 [ Time Frame: Day 7 ]Maximal concentration (Cmax)
- Pharmacokinetic parameters of OBE022/OBE002 at Day 7 [ Time Frame: Day 7 ]Half-life.
- Fœtal (cord blood)-maternal OBE002 concentration ratio at the time of delivery for patients who received IMP treatment within the previous 24 h. [ Time Frame: Day of delivery ]
- Changes in uterine contractions as assessed by electrohysterography, tocodynamometry or abdominal palpation at each hour during the first 6 hours after IMP start. [ Time Frame: Up to 6 hours after IMP start. ]
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Key Inclusion Criteria:
Part A
- Pregnant females aged ≥ 18 years
- Patients with a singleton or twin pregnancy
- Gestational age between 28 0/7 and 33 6/7
- Administered or prescribed atosiban for the treatment of preterm labour
Part B
- Pregnant females aged ≥ 18 years
- Patients with a singleton or twin pregnancy
- Gestational age between 24 0/7 and 33 6/7
- Administered or prescribed atosiban for the treatment of preterm labour
- ≥4 uterine contractions per 30 minutes
- Cervical dilatation of 1 to 4 cm inclusive
-
At least one of the following signs of preterm labour:
- positive IGFBP-1 or fœtal Fibronectin test
- cervical length ≤ 25mm
- progressive cervical change
Key Exclusion Criteria:
- Fœtal death in utero in current or previous pregnancy after gestational week 24 or expected high risk of fœtal death in the coming days
- Oligohydramnios
- Known pathological Doppler ultrasound of the umbilical artery
-
Any contraindications for the mother or the fœtus to stop labour or prolong pregnancy or any maternal or fœtal conditions likely to indicate iatrogenic delivery in the next 7 days, including but not limited to:
- Premature rupture of membranes
- Evidence or suspicion of abruptio placenta
- Signs and/or symptoms of chorio-amnionitis
- Pre-eclampsia, eclampsia or HELLP-syndrome
- Use of cervical cerclage in the current pregnancy or a pessary in situ
- Current use of anti-hypertensive medication
- Treatment with other tocolytics within specified time before the baseline assessment of uterine contractions
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03369262
Show 18 study locations
| Responsible Party: | ObsEva SA |
| ClinicalTrials.gov Identifier: | NCT03369262 |
| Other Study ID Numbers: |
17-OBE022-003 |
| First Posted: | December 11, 2017 Key Record Dates |
| Last Update Posted: | June 7, 2021 |
| Last Verified: | June 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
preterm labor preterm birth premature birth tocolysis |
prostaglandin F2α antagonist PGF2α tocolytic |
|
Premature Birth Obstetric Labor, Premature Obstetric Labor Complications Pregnancy Complications Atosiban |
Hormone Antagonists Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Tocolytic Agents Reproductive Control Agents |