Open-Label, Randomised, Active Controlled, Multi-Centre Phase 3 Study Safety and Efficacy of Danaparoid vs Argatroban (HITSOVA)

Aspen Pharmacare

Status and phase: Terminated; Phase 3

Conditions: Heparin-induced Thrombocytopenia

Treatments: Drug: Argatroban; Drug: Danaparoid Sodium

Study type: Interventional

Funder types: Industry

Identifiers

NCT03809481

ERGCR-18-ORGHIT-001

Details and patient eligibility

About

An Open-Label, Randomised, Active Controlled, Multi-Centre Phase 3 Study to Evaluate the Safety and Efficacy of Danaparoid vs Argatroban in Treatment of Subjects with Acute HIT (HITSOVA study)

Full description

Objectives:

Primary:

To show that for the treatment of subjects with acute heparin-induced thrombocytopenia (HIT) danaparoid use is not inferior to argatroban in terms of efficacy. The primary efficacy endpoint (composite endpoint) is defined as treatment response at Day 44.

A subject will be considered a treatment responder, if none of the following events occur by Day 44:

• New or extended venous and/or arterial thrombosis, including gangrene/skin necrosis Note: 'thrombosis' denotes venous and/or arterial here and throughout the protocol
• All-cause mortality
• Unplanned amputation, including ischemic gut resection

Secondary/Exploratory:

To collect additional efficacy data

• Percentage of subjects with increase in platelet count to values ≥ 100,000/ μL at day 14
• Deaths due to TE or bleeding up until Day 44
• Incidence of fatal or non-fatal major bleeding up until Day 44

Note: As outlined by the Control of Anticoagulation Subcommittee major bleeding in non-surgical subjects is defined as:

1. Fatal bleeding, and/or

2. Symptomatic bleeding in a critical area or organ, such as intracranial, intraspinal, intraocular, retroperitoneal, intra-articular or pericardial, or intramuscular with compartment syndrome, and/or

3. Bleeding causing a fall in hemoglobin level of 20 g/L (1.24 mmol/ L) or more, or leading to transfusion of two or more units of whole blood or red cells

   • New or extended thrombosis, including gangrene/skin necrosis
   • Unplanned amputation, including ischemic gut resection
   • All-cause mortality

Exploratory

• Time to first event (new/extended thrombosis, all cause mortality, unplanned amputation)
• Time to reach consistent increase in 3 consecutive alternate day platelet count measurements during acute treatment
• Incidence of new or extended TE events, including gangrene/skin necrosis up until Day 14
• Incidence of all-cause mortality up until Day 14
• Incidence of unplanned amputation up until Day 14
• Incidence of fatal or non-fatal major bleeding up until Day 14

To describe the safety of danaparoid in comparison to argatroban

• All-cause mortality
• Incidence of fatal and non-fatal major bleeding events (as defined above) during the acute treatment and then the entire follow-up period (until Day 44)
• Incidence of serious adverse events (SAEs)
• Incidence of adverse events (AEs)
• Changes in vital parameters (heart rate, blood pressure, and respiratory rate) and 12-lead electrocardiogram (ECG)
• Incidence of positive pre-danaparoid cross reactivity in the Heparin-induced Platelet Activation (HIPA) assay (Greinacher. 1991)
• Safety laboratory parameters

Design:

This is a Phase 3, open-label, randomized, active-controlled, multi-center study to evaluate the safety and efficacy of danaparoid versus argatroban in treatment of subjects with acuteHIT.

Subjects who develop a reduction in platelet count (PC) greater than or equal to 30% compared with the higher of their pre-heparin treatment count or their highest platelet count after the start of heparin either

1. Between Days 4 and 14 of the start of heparin treatment with or without thrombosis or
2. At Day 1 of heparin treatment and recent heparin exposure (within the last 30 days with or without thrombosis) and who have a score on the 4Ts test of >3 will be considered for study enrollment as a Suspected HIT.

Subjects who have tested negative in available screening tests for HIT within the last 48 hours before enrollment will not be considered for study enrollment, unless new clinical symptoms occurred.The following will occur for all subjects (regardless of whether they had a screening HIT test performed in the enrolling hospital or not):

1. All heparin administration must be ceased after strong clinical suspicion of HIT, based on clinical evaluation of the subject, including the use of heparin-bonded vascular access catheters and circuits as well as heparin flushes.
2. Subject must be randomized into the study and treated with the study drug or transferred to alternative non-heparin anticoagulant in situations where study drug cannot be started within 2 hours after stop of heparin.
3. A blood sample may be taken at the same time for HIT testing according to local practice.
4. The investigator will assess the subject for eligibility for the HITSOVA study by clinical criteria (4T score >3) and inclusion and exclusion criteria.
5. If eligible, written informed consent will be obtained from the subject or a legal guardian and the subject will be randomized to receive study drug. .
6. A new blood sample for HIPA/ PF4/heparin IgG ELISA and anti-danaparoid antibodies and cross reactivity has to be obtained to allow consistent blood sample labelling and documentation before start of study drug, regardless whether another blood sample for HIT testing according to local practice had been obtained at the time of suspicion of HIT

Note, although use of non-heparin treatment for suspected HIT is allowed before enrollment of the subject into the HITSOVA study, the study drug should be started as soon as possible, but no later than 48 hours. In such situation, all time points specified in this protocol, will be calculated from the time of first dose of study drug.

HIT diagnosis will be confirmed serologically by the HIPA assay and a specific PF4/heparin IgG ELISA test for the HIT IgG by the nominated central laboratory based in Greifswald, Germany Subjects with a positive HIPA assay and a positive HIT IgG antigen test with optical density (OD) > 0.5 will be classified as confirmed HIT, and treatment with randomized study drug will continue.Subjects with negative HIPA assay and a positive HIT IgG antigen test with an optical density (OD) >0.5 and subjects with a positive HIPA assay but a negative HIT IgG antigen test OD ≤0.5 will be classified as suspected HIT and treatment with randomized study drug will continue. These subjects will later be adjudicated retrospectively by the Adjudication Committee (AdjC) and then grouped into highly likely HIT or non-HIT.

All other subjects will be considered as non-HIT and the subjects will be removed from the protocol, study drug will be discontinued, and further procedures and treatment will be given at the discretion of the Investigator according to local standard practice. These subjects will be followed to Day 44 after their first dose of study drug for assessment of safety.

During the treatment period if it becomes necessary for an operation, invasive vascular procedure or acute kidney injury requiring the use of an extracorporeal circulation machine develops, then specific dosing instructions are available.

If the acute kidney injury does not recover during the treatment period and the use of an extracorporeal circulation machine is required longer, then the subject will not be eligible to be included in the per protocol set (PPS), but will still be eligible to be included in the full analysis set (FAS).

Study Population:

All subjects who develop a reduction in platelet count (PC) ≥ 30% compared to the higher of their pre-heparin treatment count or their highest platelet count after the start of heparin at either

a) between Days 4 and 14 of the start of heparin treatment with or without thrombosis or b) at Day 1 of heparin treatment (and recent heparin exposure within the last 30 days) with or without thrombosis and who have a score on the 4Ts test of >3 and who are later suspected HIT by the HIPA assay or HIT IgG..

Clinical signs of HIT are

• New thrombosis, on either side (arterial or venous) of the circulation

• Acute systemic reaction when heparin infusion was given:

  • Fever
  • Chills
  • High blood pressure
  • Tachycardia
  • Shortness of breath
  • Chest pain

• Transient global amnesia

• White clot syndrome

• Skin necrosis

• Occlusion of an extracorporeal circuit

Pediatric subjects will not be included in every country in this study. The countries that allow inclusion of pediatric patients are France, USA,and Italy.

It is anticipated that some subjects will be dosed with alternative non-heparin anti-coagulants prior to completing enrollment steps for this study. These subjects can be enrolled in the study as long as the exposure to those treatments is less than 48 hours.

Baseline/screening (Day 0) and enrollment into the study (Day1) can occur on the same day. In this case the assesments for Day 0 and Day 1, should only be performed once.

Enrollment: 7 patients

Sex: All

Ages: 2 weeks to 100 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

At the time of enrollment subjects are eligible to be included in the study only if all of the following criteria apply:

1. Signed written informed consent by the subject who is able to assess the nature, significance and scope of the clinical trial. If the subject is in emergency situation and temporarily incapable of consent, the consent of a legal representative or authorized representative will be waived if permitted under applicable local regulations/ethics committee recommendations. Consent must be obtained for further participation in the clinical trial as soon as this is possible and reasonable for the subject to do so to confirm understanding/willingness to participate in the clinical study and ability to comply with study procedures and the study visit schedule.

2. Males or females aged ≥2 weeks

3. Subjects with suspected HIT by 4Ts of >3 and with reduction of platelet count of ≥ 30% at either:

   1. Between Day 4 and 14 of the start of heparin exposure or
   2. At Day 1 of heparin exposure with pre-treatment with heparin within the last 30 days, with or without thrombosis.

4. Have adequate renal function: estimated glomerular filtration rate (eeGFR) ≥ 15 mL/min/1.73 m²

5. Male participants:

   A male participant must agree to use contraception during the treatment period and for at least 5 days after the last dose of study intervention and refrain from donating sperm during this period.

6. Female participants: female participant is eligible to participate if 1 of the following conditions applies:

Not a woman of childbearing potential or A woman of childbearing potential who agrees to follow the contraceptive guidance during the treatment period and during the entire VKA use and for one month after cessation of its use. Subjects should continue with adequate contraception after the study end if they continue with VKA use. (Subjects taking oral contraceptives or hormone replacement therapy must have a stable dose and regimen for ≥ 3 months prior to entry into the study.)

Exclusion Criteria:

At the time of enrollmentsubjects are excluded from the study if any of the following criteria apply:

1. Premature infants (corrected age <37 weeks gestational age)

2. Subjects undergoing Extracorporeal Membrane Oxygenation (ECMO) treatment

3. Fibrinolytic therapy <24 hours before enrollment

4. Lumbar puncture or spinal/epidural catheter placement within the past 48 hours

5. Severe hepatic impairment (Child-Pugh Class C) Note: in patients with suspected/confirmed severe liver disease, Child-Pugh C stage of liver disease must be excluded before start of treatment. For calculating Child-Pugh score, laboratory parameters in the patient file on INR, prothrombin time, serum albumin and total bilirubin taken can be taken, if they have been obtained within the last 48 hours before randomization. In all other patients these parameters have to be measured before start of treatment to identify potential exclusion criteria.

6. Active bleeding

7. Subjects with the following conditions to be excluded if alternative antithrombotic treatments are available:

   (i) Severe hemorrhagic diathesis, (ii) Traumatic damage to the central nervous system (iii) Brain, spinal or ophthalmologic surgery (iv) Active stomach/duodenal ulcers or active peptic ulcer unless this ulcer is the cause of the surgical procedure

8. An unexplained activated partial thromboplastin time (aPTT) > 2 x the normal range

9. A hemorrhagic cerebrovascular accident within the previous 3 months

10. Severe, uncontrolled hypertension defined as blood pressure >180/110 mmHg

11. Diabetic retinopathy

12. Acute bacterial endocarditis

13. Expectation of a long-term (> 3 weeks) hemodialysis requirement before the end of the acute treatment

14. Hypersensitivity to the active substances or to any of the excipients

15. Hypersensitivity to sulphite

16. Any investigational drug(s) use within 4 weeks preceding screening or anticipated use during the course of the study

17. Pregnant or breastfeeding woman

18. Use of intra-aortic balloon pump, or ventricular assist device

19. Use of any non-heparin anticoagulant treatment for suspected HIT for more than 48 hours before enrollment.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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7 participants in 2 patient groups

Danaparoid Sodium

Experimental group

Description:

Subjects will receive danaparoid via IV infusion for at least 7 days then transition to a VKA. IV loading bolus injection of 2250 U, followed by 400 U/h for 4 hours, then 300 U/h for 4 hours, then a maintenance infusion of 150-200 U/h.

Treatment:

Drug: Danaparoid Sodium

Argatroban

Active Comparator group

Description:

Subjects will receive argatroban 2 microgram/kg/min as a continuous infusion, titrated to an aPTT that is 1.5 to 3.0 x initial baseline value, but not exceeding 100 seconds.

Treatment:

Drug: Argatroban