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RecruitingNCT07205861TWILIGHTUpdated Oct 3, 2025

Retrospective Epidemiological Study of Patients in the National Cohort of the French TMA Center

An observational study in Thrombotic Thrombocytopenic Purpura (TTP), Immune Thrombotic Thrombocytopenic Purpura and Thrombotic Microangiopathies, sponsored by Assistance Publique - Hôpitaux de Paris. Recruiting at 1 site in France. Per ClinicalTrials.gov, last updated 2025-10-03.

Sponsored by Assistance Publique - Hôpitaux de Paris · Observational

From the registry’s dates

  • Started Dec 2024; still recruiting 1 year 11 months later.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
1,200
Sex
All
01

Study summary

Immune thrombotic thrombocytopenic purpura (iTTP) is a rare, life-threatening disorder characterized by microangiopathic hemolytic anemia, severe thrombocytopenia, and ischemic organ damage due to microvascular thrombosis. It results from a severe deficiency in the von Willeband factor (vWF)-cleaving protease ADAMTS13, primarily caused by autoantibodies that inhibit its activity. This deficiency leads to accumulation of ultra-large vWF multimers, triggering pathological platelet aggregation and widespread microthrombi. iTTP typically presents with acute neurological symptoms (e.g., confusion, seizures, coma), cardiac events (e.g., myocardial infarction), and multiorgan dysfunction. Without prompt treatment-plasma exchange, immunosuppression, and the vWF inhibitor caplacizumab-mortality exceeds 90%. Survivors face long-term risks, including cardiovascular complications, cognitive impairment, and reduced life expectancy.

The TWI-LIGHT protocol is a national retrospective epidemiological study coordinated by the French Reference Center for Thrombotic Microangiopathies (CNR-MAT). It aims to analyze long-term outcome in >1,200 iTTP patients diagnosed between October 2000 and June 2024. The study leverages pseudonymized data from the CNR-MAT registry, collected via a secure REDCap database.

Key Objectives:

  1. Primary: Assess the impact of cardiovascular risk factors (e.g., hypertension, diabetes) and ADAMTS13 activity on life expectancy in iTTP survivors.
  2. Secondary:

    • Evaluate disease burden in underrepresented groups (pregnant/postpartum women, children, elderly patients).
    • Analyze the influence of new therapies (caplacizumab, rituximab, recombinant ADAMTS13) on care pathways.
    • Identify prognostic factors and treatment practices.
    • Characterize neurocognitive outcomes and quality of life post-iTTP.

Methodology:

  • Design: Non-interventional, retrospective (MR-004 compliance), using data from standard care.
  • Inclusion: Patients with confirmed iTTP (thrombocytopenia, hemolytic anemia, ADAMTS13 \<10%), diagnosed within the study period, and ≥1 year of follow-up.
  • Exclusion: Cancer-associated iTTP, severe sepsis, or patient opposition to data reuse.
  • Data Collection: Clinical, biological, and therapeutic variables from hospital/consultation records, including cardiovascular events, ADAMTS13 activity, and neurocognitive assessments.
  • Analysis: Kaplan-Meier survival curves and Cox regression models to identify risk factors for non-iTTP-related death.

Expected Outcomes:

  • Prevalence of cardiovascular comorbidities and their correlation with ADAMTS13 activity.
  • Insights into iTTP subtypes (e.g., gestational, pediatric) and therapeutic efficacy.
  • Evidence-based strategies for personalized long-term management.

Ethical Framework:

  • AP-HP-sponsored, with oversight from Sorbonne University's ethics committee.
  • Patients informed of data reuse with opt-out rights; data archived for 15 years.

This landmark study will inform clinical guidelines, optimize survivor care, and address unmet needs in iTTP management through comprehensive, real-world data analysis.

Read the detailed description

The TWI-LIGHT protocol is a retrospective, non-interventional epidemiological study coordinated by the French National Reference Center for Thrombotic Microangiopathies (CNR-MAT). It leverages the CNR-MAT registry to analyze long-term outcomes in over 1,200 patients diagnosed with autoimmune thrombotic thrombocytopenic purpura (iTTP) between October 1, 2000, and June 1, 2024.

Background and Rationale iTTP is a rare, life-threatening disorder caused by severe ADAMTS13 deficiency, leading to microvascular thrombosis, multiorgan damage, and high mortality without prompt treatment. Survivors face long-term risks, including cardiovascular complications, cognitive impairment, and reduced life expectancy. Despite therapeutic advances (e.g., caplacizumab, rituximab), data on late complications, risk factors, and disease burden in underrepresented subgroups (e.g., pregnant women, children, elderly patients) remain limited. This study addresses critical gaps in understanding iTTP's natural history, treatment efficacy, and survival.

Study Design

  • Type: Retrospective, multicenter, non-interventional (MR-004 compliance).
  • Data Collected:

    • Acute Phase: Clinical presentation, lab results (standard biology, including ADAMTS13 activity, troponin), treatments (plasma exchange, immunosuppressants, caplacizumab).
    • Long-Term Follow-Up: Cardiovascular events (major adverse cardiovascular events, including ischemic stroke, myocardial infarction and angioplasty) and cardiovascular risk factors (hypertension, diabetes, weight and body mass index, dyslipidemia, smoking), ADAMTS13 activity trends, neurocognitive outcomes (quality-of-life scales: SF36, HADS), relapse rates, and mortality.
  • Biobanking: ADAMTS13 samples stored at Hôpital Lariboisière (Prof. Veyradier's lab) under ethical approval (AC-2023-6021).

Expected Outcomes and Impact

  • Clinical Insights:

    • Personalized cardiovascular risk profiles for iTTP survivors.
    • Evidence-based guidelines for pregnancy, elderly, and pediatric iTTP management.
    • Optimization of long-term monitoring (e.g., rituximab frequency).
  • Health System Impact:

    • Cost-benefit analysis of novel therapies (e.g., caplacizumab, recombinant ADAMTS13).
    • Strategies to reduce diagnostic delays and hospitalizations. Real-World Relevance: Focus on underrepresented groups and long-term survival, with the goal to improve life expectancy of iTTP patients. This protocol represents a landmark effort to transform iTTP management through comprehensive real-world data, directly impacting clinical practice.
  • Methodological Rigor: Centralized data auditing, ISO/IEC 17025-compliant biobanking.
02

Conditions studied

  • Thrombotic Thrombocytopenic Purpura (TTP)
  • Immune Thrombotic Thrombocytopenic Purpura
  • Thrombotic Microangiopathies
  • Microangiopathy, Thromboic
  • Cardiovascular Diseases
  • Autoimmune Diseases
  • Rare Diseases
  • Neurological Manifestations

Keywords

  • Thrombotic Thrombocytopenic Purpura
  • Immune Thrombotic Thrombocytopenic Purpura
  • Thrombotic Microangiopathies (MeSH: D057049)
  • Microangiopathies, Thrombotic (MeSH: D057172)
  • ADAMTS13 Protein (MeSH: C423082)
  • Autoimmune Diseases (MeSH: D001327)
  • Cardiovascular Diseases (MeSH: D002318)
  • Epidemiologic Studies (MeSH: D004812)
  • Retrospective Studies (MeSH: D012196)
  • Observational Study (Publication Type)
  • Risk Factors (MeSH: D012307)
  • Treatment Outcome (MeSH: D016647)
  • Rare Diseases (MeSH: D034381)
  • Longitudinal Studies (MeSH: D008159)
  • Patient Registry (MeSH: D010329)
  • Survival (MeSH: D009505)
  • Quality of Life (MeSH: D011788)
  • Neurological Manifestations (MeSH: D009462)
03

In context

Purpura, Thrombotic Thrombocytopenic

67 studies on the registry are indexed under Purpura, Thrombotic Thrombocytopenic; 18 are open to participants now.

This study's planned enrollment of 1,200 is above the median of 156 across 27 observational studies indexed under Purpura, Thrombotic Thrombocytopenic.

Browse Purpura, Thrombotic Thrombocytopenic studies →

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,592 studies on the registry; 1,033 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population consists of all patients in France diagnosed with thrombotic thrombocytopenic purpura (TTP), primarily the autoimmune subtype, between October 1, 2000, and June 1, 2024, who received care within the national network of the French Reference Center for Thrombotic Microangiopathies (CNR-MAT). This includes adults and children with autoimmune who have at least one year of follow-up. Patients are recruited from 6 core and 25 competence centers covering mainland France and overseas territories, ensuring nationwide representation. Data are collected from hospital and consultation records, and only patients who do not object to data reuse are included. This approach ensures a comprehensive, multicentric, and representative cohort for rare disease research.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

-Patients with a diagnosis of immune mediated TTP

Exclusion criteria

Exclusion Criteria:

  • Cancer- associated iTTP and -associated iTTP
  • Severe sepsis
  • Disseminated intravascular coagulation with consumption of coagulation factors;
  • Transplant-associated TTP
  • HIV-associated TTP (AIDS stage)
  • Patient not affiliated with a social security scheme
  • Patient or parent's objection to the reuse of their healthcare data for research
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
1,200 participants (estimated)
Patient registry
No

Groups and cohorts

  • iTTP patients

    The study is structured around one main cohort of all patients with immune thrombotic thrombocytopenic purpura (iTTP). Subgroup analyses are planned for specific populations: pregnant and postpartum women, pediatric patients, and elderly patients. There are no separate intervention or control groups; the design is a single retrospective cohort with multiple subgroup analyses.

06

What researchers measure

Primary outcomes

  1. prevalence of major cardiovascular events

    ischemic strocke, myocardial infarction, reperfusion/angioplasty

    Time frame: from diagnosis to last follow- up, up to 3 years

Secondary outcomes

  1. Incidence of cardiovascular risk factors

    Hypertension, diabetes, dyslipidaemia, smocking, body mass index,

    Time frame: from diagnosis to last follow- up, up to 3 years

  2. correlation between ADMTS13 activity during remission and incidence of cardiovascular events and life expectancy

    Time frame: from remission to last follow- up, up to 3 years

  3. characterization of pregnancy onset iTTP

    clinical presentation, management, prognosis(specific characteristics )

    Time frame: from diagnosis to last follow- up, up to 3 years

  4. characterization of childhood onset iTTP

    clinical presentation, management, prognosis(specific characteristics )

    Time frame: from diagnosis to last follow- up, up to 3 years

  5. characterization of elderly onset iTTP

    clinical presentation, management, prognosis(specific characteristics )

    Time frame: from diagnosis to last follow- up, up to 3 years

07

Study locations

1 of 1 sites recruiting
  • Service d'Hématologie Hôpital Saint-Antoine
    Paris, 75012, France
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07205861
Responsible party
Sponsor
First posted
Oct 3, 2025
Start date
Dec 2, 2024
Primary completion
Dec 2027 (estimated)
Completion
Dec 2028 (estimated)
Last update
Oct 3, 2025

Study contacts

Paul COPPO, MD, PHD
Contact
aul.coppo@aphp.fr
00 33 1 49 28 34 39
Paul COPPO, MD, PHD
principal investigator · Assistance Publique - Hôpitaux de Paris

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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