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Pulmonary Arterial HypertensionPhase 4NCT02893995

Safety, Tolerability, Pharmacokinetics and Efficacy of Two Different Rates of Subcutanous Remodulin® Dose Titration in Pulmonary Arterial Hypertension

A Phase 4 study testing Slow Dose Titration Group of Subcutaneous Treprostinil and Rapid Dose Titration Group of Subcutaneous Treprostinil in people with Pulmonary Arterial Hypertension, run by United Therapeutics at 10 sites in China.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

This is an open-label, multicenter, parallel, randomized (1:1 Slow Dose Titration Group; Rapid Dose Titration Group), two-group study to evaluate the safety, tolerability, pharmacokinetics and efficacy of slow and rapid dose titration regimens of subcutaneous Remodulin infusion in subjects with pulmonary arterial… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Pulmonary Arterial Hypertension
What is being tested?
Slow Dose Titration Group of Subcutaneous Treprostinil and Rapid Dose Titration Group of Subcutaneous Treprostinil
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
10 sitesChina
Study dates
Feb 2017to Apr 2018
Phase
Phase 4
Are there results?
None posted in the registry

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
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • A subject is eligible for inclusion in this study if all of the following criteria apply:
  • The subject voluntarily gives written informed consent to participate in the study.
  • The subject is at least 18 years of age at screening.
  • The subject weighs a minimum of 40 kg with a body mass index less than 40 kg/m2 at screening.
  • The subject has a diagnosis of idiopathic or heritable PAH, PAH associated with repaired congenital systemic-to-pulmonary shunts (at least one year since repair with respect to the date of providing informed consent), or PAH associated with connective tissue diseases.
  • The subject must have a baseline 6MWD between 150 and 550 meters, inclusive, in the absence of a concurrent injury, illness (other than PAH or a PAH related condition), or other confounding factor that would prevent the accurate assessment of the subject's exercise capacity.
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  • The subject is either treatment naïve or is receiving a PDE-5 inhibitor and/or an ERA for at least 60 days prior to screening and on a stable dose for at least 30 days prior to screening and is willing to remain on a PDE-5 inhibitor and/or an ERA at the same dose for the duration of the 16-week treatment phase.
  • The subject must be optimally treated with conventional pulmonary hypertension therapy (e.g., oral vasodilators, oxygen, digoxin, etc.) with no additions, discontinuations, or dose changes for at least 14 days prior to screening (excluding diuretics and anticoagulant dose adjustments).
  • The subject has undergone right heart catheterization during the screening period (or within 3 years before screening) and been documented to have a mean pulmonary artery pressure (PAPm) of greater than or equal to 25 mmHg, a pulmonary arterial wedge pressure (PAWP) of less than or equal to 15 mmHg, and pulmonary vascular resistance (PVR) of more than 3 Wood units.
  • The subject has undergone echocardiography within 7 days prior to randomisation with evidence of clinically normal left systolic and diastolic ventricular function, absence of any clinically significant left sided heart disease (e.g., mitral valve stenosis) and absence of unrepaired congenital heart disease. Subjects with clinically insignificant left ventricular diastolic dysfunction due to the effects of right ventricular overload (i.e., right ventricular hypertrophy and/or dilatation) will not be excluded.
  • The subject has a previous ventilation perfusion lung scan and/or high resolution computerized tomography scan of the chest and/or pulmonary angiography that are consistent with the diagnosis of PAH (e.g., low probability of pulmonary embolism; absence of major perfusion defects).
  • The subject has pulmonary function tests done within 9 months prior to or during the screening period with the following:
  • Total lung capacity (TLC) is at least 60% (of predicted value)
  • Forced expiratory volume in one second/forced vital capacity (FEV1/FVC) ratio is at least 50%
  • Sexually active women of childbearing potential must practice true abstinence from intercourse when it is in line with their preferred and usual lifestyle, or use two different forms of highly effective contraception. Medically acceptable forms of effective contraception include: (1) approved hormonal contraceptive (such as birth control pills), (2) barrier methods (such as a condom or diaphragm) used with a spermicide, (3) an intrauterine device (IUD), or (4) partner vasectomy. For women of childbearing potential, a negative serum pregnancy test is required at screening and a negative hCG urine pregnancy test is required at baseline visit. Women of child bearing potential include any females who have experienced menarche and who have not undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation or bilateral oophorectomy) or are not postmenopausal (defined as amenorrhea for at least 12 consecutive months).
  • Males participating in the study must use a condom during the length of the study, and for at least 48 hours after discontinuing study medication.
  • In the opinion of the Principal Investigator, the subject is able to communicate effectively with study personnel, is considered reliable, willing and likely to be cooperative with protocol requirements, including attending all study visits, and is mentally and physically capable of learning to administer Remodulin by continuous SC infusion using a micro infusion pump.

Who cannot join

  • A subject is not eligible for inclusion in this study if any of the following criteria apply:
  • The subject is pregnant or lactating.
  • The subject has received epoprostenol, treprostinil, iloprost or beraprost within 90 days prior to screening (except if used during acute vasoreactivity testing).
  • The subject has had previous intolerance or lack of efficacy to prostacyclin or a prostacyclin analogue that resulted in discontinuation or inability to titrate that therapy effectively.
  • The subject has any disease associated with PH other than idiopathic or heritable PAH, or PAH associated with repaired (for at least one year) congenital systemic-to-pulmonary shunts or connective tissue diseases or has had an atrial septostomy.
  • The subject is in WHO functional class IV.
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  • The subject has a current diagnosis of uncontrolled sleep apnea as defined by their physician.
  • The subject has liver function tests (AST or ALT) greater than three times the upper limit of the laboratory reference range.
  • The subject has a history of active gastro-intestinal ulcer, intracranial hemorrhage, injury or other cause of clinically significant bleeding episode within 6 months before screening, or any other disease / condition that would either jeopardize the safety of the subject and / or interfere with the interpretation of study assessments in the opinion of the Investigator.
  • The subject has a history of ischemic heart disease including previous myocardial infarction or symptomatic coronary artery disease within 6 months before screening, or history of left sided myocardial disease as evidenced by a PAWP (or left ventricular end-diastolic pressure) greater than 15 mmHg or left ventricular ejection fraction (LVEF) less than 40%.
  • The subject has uncontrolled systemic hypertension as evidenced by systolic blood pressure greater than 160 mmHg or diastolic blood pressure greater than 100 mmHg.
  • The subject has systemic hypotension as evidenced by systolic blood pressure less than 85 mmHg
  • The subject has a musculoskeletal disorder (e.g., arthritis affecting the lower limbs, recent hip or knee joint replacement, artificial leg) or any other disease that is likely to limit ambulation, or is connected to a machine that is not portable.
  • The subject has an unstable psychiatric condition or is mentally incapable of understanding the objectives, nature, or consequences of the trial, or has any condition which in the Investigator's opinion would constitute an unacceptable risk to the subject's safety.
  • The subject is receiving an investigational drug, has an investigational device in place or has participated in an investigational drug or device study within 30 days prior to screening.

Trial locations and contacts

10 sites in 1 country.

10 sites in 1 country

China10 sites

  • Beijing Chao-Yang Hospital

    Beijing, 100020

  • Beijing Anzhen Hospital, Capital Medical University

    Beijing, 100029

  • Peking Union Medical College Hospital

    Beijing, 100032

  • Fu Wai Hospital

    Beijing, 100037

  • Beijing Shijitan Hospital

    Beijing, 100038

  • Xiangya Hospital Centre South University

    Changsha, 410008

  • Guangdong General Hospital

    Guangzhou, 510080

  • Zhongshan Hospital affiliated with Fudan University

    Shanghai, 200032

  • Shanghai Pulmonary Hospital

    Shanghai, 200433

  • Wuhan Asia Heart Hospital

    Wuhan, 430022

Other trials in China

About this study

Official title: A 16-Week, Open-Label, Multi-Center, Parallel, Randomized Controlled Study to Compare the Safety, Tolerability, Pharmacokinetics and Efficacy of Slow and Rapid Dose Titration Regimens of Subcutaneous Remodulin Therapy in Subjects With Pulmonary Arterial Hypertension

This is an open-label, multicenter, parallel, randomized (1:1 Slow Dose Titration Group; Rapid Dose Titration Group), two-group study to evaluate the safety, tolerability, pharmacokinetics and efficacy of slow and rapid dose titration regimens of subcutaneous Remodulin infusion in subjects with pulmonary arterial hypertension (PAH). The study will include about 50 subjects at up to 10 clinical trial centers in China. The treatment phase of the study will last approximately 16 weeks. Subjects who complete all required assessments will also be eligible to enter a long-term open-label, extension study (CVT-CV-004).

Being tested
Slow Dose Titration Group of Subcutaneous Treprostinil, Rapid Dose Titration Group of Subcutaneous Treprostinil
Keywords
PAH, Subcutaneous Treprostinil, Remodulin, 6 Minute Walk Test
Medical subject headings
Pulmonary Arterial Hypertension

What participants receive

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

  • Slow Dose Titration Group of Subcutaneous TreprostinilDrug

    Also called Remodulin

    subcutaneous treprostinil

  • Rapid Dose Titration Group of Subcutaneous TreprostinilDrug

    Also called Remodulin

    subcutaneous treprostinil

Study groups in NCT02893995
Study groupRoleWhat they receive
Slow Dose Titration Group of Subcutaneous TreprostinilExperimentalRemodulin (1.0, 2.5, 5 and 10 mg/ml formulations as available) will be administered by continuous subcutaneous infusion via a subcutaneous cannula using a microbore infusion tubing set and a micro infusion pump. While hospitalized, initiation will begin at approximately 1.25 ng/kg/min of subcutaneous treprostinil with dose increases of approximately 1.25 ng/kg/min once every seven days for the first 4 weeks, then approximately 2.5 ng/kg/min every seven days thereafter according to clinical response and tolerability.
Receives: Drug: Slow Dose Titration Group of Subcutaneous Treprostinil
Rapid Dose Titration Group of Subcutaneous TreprostinilExperimentalRemodulin (1.0, 2.5, 5 and 10 mg/ml formulations as available) will be administered by continuous subcutaneous infusion via a subcutaneous cannula using a microbore infusion tubing set and a micro infusion pump. While hospitalized, initiation will begin at approximately 2.0 ng/kg/min with dose increments of 1-2 ng/kg/min approximately every 12 hours according to clinical response and tolerability. Following subject discharge, the dose rate should be increased by 1-2 ng/kg/min with dose increments separated by at least 24 hours. When a dose rate of 20 ng/kg/min has been achieved the dose increments can be increased up to 4 ng/kg/min with dose increments separated by at least 24 hours. The aim is to achieve a dose rate of at least 10, 20, 30 and 40 ng/kg/min by the end of Weeks 1, 4, 8 and 12, respectively.
Receives: Drug: Rapid Dose Titration Group of Subcutaneous Treprostinil

What is being measured

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

  1. Incidence of Adverse Events Among Subjects through 16 Weeks

    The incidence of adverse events among subjects throughout the 16 week study will be measured by the number of subjects analyzed and the percentage of those subjects who experienced an adverse event.

    Measured: 16 Weeks

  2. Change in Patient Reported Site Pain from Baseline to Week 16

    The site pain questionnaire is a 10-point scale rating the worst site pain experienced on a measured day. Scores will range from 0 (no pain) to 10 (worst possible pain). The questionnaire will be completed each time a new infusion site is placed and until a subject's infusion site pain level reaches a score of zero for two consecutive days or they have completed 14 days. Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Baseline and Week 16

  3. Incidence of Subject Discontinuations Among Participants through 16 Weeks

    The incidence of subject discontinuations among subjects throughout the 16 week study will be measured by the number of subjects analyzed and the percentage of those participants who discontinued.

    Measured: 16 Weeks

Secondary outcomes (9)

  1. Change in 6-minute Walk Distance (6MWD) from Baseline to Week 16

    The intent of the 6MWD test is to evaluate exercise capacity associated with carrying out activities of daily living. Change in 6MWD from Baseline to Week 16, correlates with the current clinical standard for assessing patient functional status in the treatment of PAH and is considered an objective measure of patient functional status by the American Thoracic Society (ATS). Subjects will be instructed to walk down a corridor at a comfortable speed as far as they could manage for six minutes. Distance <500 meters suggests considerable exercise limitation; Distance 500-800 meters suggests moderate limitation; Distance >800 meters (with no rests) suggests mild or no limitation. Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Baseline and Week 16

  2. Change in Borg Dyspnea Score (following 6MWT) from Baseline to Week 16

    The Borg dyspnea score is a 10-point scale rating the maximum level of dyspnea (difficulty in breathing) experienced during the six-minute walk test (6MWT). The Borg dyspnea score will be assessed immediately following the 6MWT. Scores range from 0 (for no shortness of breath) to 10 (for the greatest shortness of breath ever experienced). Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Baseline and Week 16

  3. Change in N-terminal pro-B-type natriuretic peptide (NT-proBNP) concentrations from Baseline to Week 16

    The N-terminal pro-BNP (NT-proBNP) serum concentration will be assessed as a biomarker to compare the severity of heart failure at Baseline and Week 16. Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Baseline and Week 16

  4. Number of Participants with a Change from Baseline World Health Organization (WHO) Functional Classification at Week 16

    The WHO Functional Class of pulmonary hypertension is a physical activity rating scale as follows: Class I: No limitation of physical activity. Class II: Slight limitation of physical activity. Class III: Marked limitation of physical activity. Class IV: Inability to carry out any physical activity without symptoms. Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Change from Baseline at Week 16

  5. Change in PAH Symptoms from Baseline to Week 16

    Symptoms of PAH including fatigue, dyspnea, edema, dizziness, syncope, chest pain and orthopnea will be assessed and if present, the intensity of the symptom will be rated as mild, moderate, or severe. Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Change from Baseline at 16 Weeks

  6. Change in Measured Tricuspid Annular Plane Systolic Excursion (TAPSE) from Baseline to Week 16

    Change in right ventricular function will be assessed using the tricuspid annular plane systolic excursion (TAPSE) as determined by echocardiography. Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Baseline and Week 16

  7. Change in Measured Tricuspid Regurgitant Jet Velocity (TRJV) from Baseline to Week 16

    Change in right ventricular function will be assessed using the tricuspid regurgitant jet velocity (TRJV) as determined by echocardiography. Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Baseline and Week 16

  8. Incidence of Pericardial Effusion from Baseline to Week 16

    Change in right ventricular function will be assessed by the presence or absence of pericardial effusion as determined by echocardiography. Changes from Baseline to Week 16 will be summarized and compared between treatment groups using descriptive statistics. No formal hypothesis testing will be performed.

    Measured: Baseline and Week 16

  9. Measure treprostinil plasma concentration from Week 4 to Week 16

    During the treatment phase at Weeks 4, 8, 12, and 16 or at the time of premature study termination, a single blood sample will be collected to measure treprostinil plasma concentration.

    Measured: Week 4, Week 8, Week 12, and Week 16

Timeline

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

  1. First posted9 Sep 2016 (estimated)
  2. Study startFeb 2017 (estimated)
  3. Primary completionApr 2018 (estimated)
  4. Study completionApr 2018 (estimated)

Why it stopped: Business decision

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 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02893995
Sponsor's protocol ID
CVT-CV-003
Status last verified
May 2017
First submitted
24 Aug 2016
Last updated
9 May 2017
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Slow Dose Titration Group of Subcutaneous Treprostinil and Rapid Dose Titration Group of Subcutaneous Treprostinil in people with Pulmonary Arterial Hypertension, run by United Therapeutics at 10 sites in China.

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 17 inclusion and 15 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: withdrawn, as of the sponsor's last update on 9 May 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 10 sites in China. 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 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

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

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

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?

Incidence of Adverse Events Among Subjects through 16 Weeks (time frame: 16 Weeks). The study lists 3 primary outcomes in all. 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 NCT02893995.

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 9 May 2017.

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