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The Fifth INTEnsive pReventing Secondary Injury in Acute Cerebral Haemorrhage Trial Within ACT-GLOBAL (INTERACT5)

T

The George Institute

Status and phase

Enrolling
Phase 3

Conditions

Supratentorial Intracerebral Haemorrhage
Acute Intracerebral Haemorrhage
Intracerebral Hemorrhage
Acute Stroke
Spontaneous Intracerebral Hemorrhage

Treatments

Drug: Colchicine 0.5 mg
Other: Control (Standard treatment)
Drug: Deferoxamine Mesylate

Study type

Interventional

Funder types

Other

Identifiers

NCT06763055
ACT-GLOBAL_ICH_01

Details and patient eligibility

About

This is a domain within the ACT-GLOBAL platform trial to compare the effectiveness of early and appropriate pharmacological interventions in acute intracerebral hemorrhage (ICH) to control secondary brain injury. Up to 2000 patients with presumed spontaneous supratentorial intracerebral hemorrhage (ICH) will be followed for 6 months (or death, if prior to 6 months).

Adaptive interim analyses will be used, with statistical triggers to determine if any of the interventions are superior to control. The end of the trial is defined as the date that all participants have completed their 6-month assessment.

A large amount of preclinical data indicates that the outcome from ICH is linked to the detrimental effects of breakdown substances from brain bleeds. However, there remains a lack of compelling evidence supporting the effectiveness of any pharmacological intervention that can mitigate the secondary cerebral injury. The INTERACT domain aims to assess the effectiveness of intravenous deferoxamine and low-dose oral colchicine, both individually and in combination, to standard of care alone, on improving functional outcome in patients with spontaneous supratentorial ICH.

Those patients who meet eligibility criteria will be randomized to receive one of four interventions:

  1. No deferoxamine mesylate and no colchicine (labeled as control)
  2. Deferoxamine mesylate only: deferoxamine mesylate at a dose of 32mg/kg/day via intravenous infusion immediately (within 1 hour) post-randomization and continue for the following 2 consecutive days.
  3. Colchicine only: 0.5mg of oral colchicine daily for 30 consecutive days.
  4. Both deferoxamine mesylate and colchicine: deferoxamine mesylate at a dose of 32mg/kg/day via intravenous infusion immediately (within 1 hour) post-randomization and continue for the following 2 consecutive days; plus 0.5mg of oral colchicine daily for 30 consecutive days.

Full description

Intracerebral hemorrhage (ICH) is a severe type of stroke, responsible for substantial disability and death worldwide. It accounts for 6.5% to 19.6% of all strokes, with incidence rates increasing, especially in low- and middle-income countries. Survivors often face significant consequences, including functional impairments, recurrent strokes, cognitive decline, and depression.

Despite advancements in acute stroke care, there are few effective treatments specifically targeting the brain damage caused by ICH. Previous research has identified that the formation of perihaematomal oedema (PHE) is a critical factor in poor recovery, making it a key focus for therapeutic development.

INTERACT5 domain will focus on two promising medications. Deferoxamine, an iron-chelating agent, targets oxidative stress caused by iron released from damaged brain tissue. Studies suggest it may reduce brain swelling and secondary injury after ICH. Colchicine, an anti-inflammatory medication, inhibits pathways involved in inflammation, which may help minimize brain damage. INTERACT5 will enroll patients aged 18-80 with acute spontaneous supratentorial ICH, confirmed through imaging, who present to the hospital within 24 hours of symptom onset. Other domain-specific inclusion criteria:

  • Hematoma volume ≥≥10 mL or any volume post-surgery
  • NIHSS score >8
  • GCS ≥8>7

Participants will be randomized to one of four groups: standard care, deferoxamine alone, colchicine alone, or both treatments combined. Deferoxamine will be administered intravenously (32 mg/kg/day within 1 hour and continued for 2 consecutive days), and colchicine will be given orally (0.5 mg daily for 30 days).

The study's primary outcome is the improvements in functional outcomes at 6 months, measured by the modified Rankin Scale (mRS). Secondary outcomes include EQ-5D-5L at 6 months, changes in PHE size, NIHSS scores, length of hospital stay, ambulatory status at discharge and safety indicators such as mortality at 6 months/SAEs to 6 month, kidney and liver function.

Response Adaptive Randomization (RAR) will be used in this domain to allow readjustment of recruitment towards treatment arms with more favorable emerging effects. Randomization will use minimization method to minimize the imbalance between the number of patients in each treatment group over a number of factors including region, location (deep vs cortical)age (>65 vs ≤65 years old), sex (male vs female), time from onset (>6 vs ≤6 hours), haematoma volume (10-29 vs ≥30 mL), receipt of any decompressive surgery (yes vs no), and intraventricular extension of ICH, etc.

Enrollment

2,000 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age between 18 and 80 years old
  2. Diagnosis of presumed spontaneous supratentorial intracerebral haemorrhage, confirmed by brain imaging
  3. Presentation to hospital within 24 hours of symptom onset (or last seen well)
  4. Hematoma volume ≥10 mL or any volume post-surgery
  5. NIHSS score >8
  6. GCS ≥8
  7. Provide written informed consent by patient (or approved surrogate)

Exclusion criteria

  1. Secondary cause of haemorrhage (e.g., structural abnormality such as arteriovenous malformation, cerebral aneurysm, tumour, trauma), or haemorrhagic transformation of acute ischaemic stroke

  2. Isolate intraventricular haemorrhage

  3. Chronic Kidney Disease

  4. Very high likelihood of death within 7 days or poor adherence to study treatment or follow-up

  5. Severe comorbid disease that will interfere with outcome assessments (e.g., cancer, chronic airflow disease, heart failure, significant disability)

  6. Women who are pregnant or lactating

    Exclusion Criteria related to use of deferoxamine:

  7. Previous chelation therapy or known hypersensitivity to deferoxamine products;

  8. Severe iron deficiency anaemia (haemoglobin <7 g/dL or requiring regular blood transfusions);

  9. Taking iron supplements containing >325 mg of ferrous iron;

  10. Serum creatinine >2 mg/dL;

  11. Patients with known heart failure taking >500 mg of vitamin C

    Exclusion criteria related to the use of colchicine:

  12. Allergic to colchicine

  13. Myelodysplastic hypoplasia, or liver or severe renal failure

  14. Use of medication which may interact with colchicine (e.g., strong CYPsA4 inhibitors such as ketoconazole, strong P-glycoprotein inhibitors such as fluconazole)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

2,000 participants in 4 patient groups, including a placebo group

No deferoxamine mesylate, No colchicine (control)
Placebo Comparator group
Description:
The group will not receive deferoxamine mesylate or colchicine
Treatment:
Other: Control (Standard treatment)
Deferoxamine mesylate only
Active Comparator group
Description:
The intervention group will receive deferoxamine mesylate at a dose of 32mg/kg/day via intravenous infusion immediately (within 1 hour) of randomization and continued for 2 consecutive days.
Treatment:
Drug: Deferoxamine Mesylate
Colchicine only
Active Comparator group
Description:
The intervention group will receive 0.5mg of oral colchicine daily as soon as possible after randomization, to continue for 30 days.
Treatment:
Drug: Colchicine 0.5 mg
Both deferoxamine mesylate and colchicine
Active Comparator group
Description:
The intervention group will receive deferoxamine mesylate at a dose of 32mg/kg/day via intravenous infusion immediately (within 1 hour) and continued for 2 consecutive days; plus 0.5mg of oral colchicine daily as soon as possible after randomization, to continue for 30 days.
Treatment:
Drug: Deferoxamine Mesylate
Drug: Colchicine 0.5 mg

Trial contacts and locations

2

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Central trial contact

Xiaoying Chen, PhD BPharm BMgt; Craig Anderson, MD

Data sourced from clinicaltrials.gov

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