Disease × agent evidence record

Anti-Thymocyte Globulin for Immune Thrombocytopaenia (ITP): evidence, trials and status

Trials of Anti-Thymocyte Globulin in Immune Thrombocytopaenia (ITP) are registered but none has completed, so there is no outcome evidence from those studies yet; the record is a signal of research interest.

1 registered trials 0 recruiting 0 publications Evidence tier A · Strong Score 21.0
Research Tracker › Pairs › Immune Thrombocytopaenia (ITP) › Anti-Thymocyte Globulin
Research map, not treatment advice. This page aggregates registry and literature records. It does not evaluate efficacy, dosing or safety for any individual. Discuss any treatment decision with a qualified clinician.

Summary

Anti-Thymocyte Globulin has reached the approved stage (maximum clinical phase 4) for at least one indication, so its use in Immune Thrombocytopaenia (ITP) would be drug repurposing rather than first-in-human development. This does not mean it is approved for Immune Thrombocytopaenia (ITP). ClinicalTrials.gov lists 1 registered trial linking Anti-Thymocyte Globulin to Immune Thrombocytopaenia (ITP): 1 is terminated, withdrawn, suspended or of unknown status. None of the registered studies carries a drug-development phase label, which is typical for behavioural, device and supplement protocols. It plans or enrolled 10 participants. Registered activity dates to 2000. No published literature item is linked to Anti-Thymocyte Globulin and Immune Thrombocytopaenia (ITP) in the OSMF database yet, so the record rests on registry entries alone. Registry entries describe intent to study, not outcomes.

The RepurpOS disease-intelligence file for Immune Thrombocytopenia ranks 50 candidate therapeutics from Open Targets, ChEMBL, DGIdb and PubMed; only a minority carry direct clinical evidence, and this page covers one of those. Spontaneous remission context recorded for the condition: Childhood ITP: spontaneous remission in 70-80% within 6 months; Adult ITP: spontaneous remission in 20-30% at 1 year without treatment; chronic ITP (>12 months) rarely resolves spontaneously.

Evidence table

Evidence tierA · Strong
Evidence score21.0 (trials 1.0, literature 0.0, tier 15, approved bonus 5.0)
Registered trials1 total: 0 recruiting, 0 active / not yet recruiting, 0 completed, 1 other
Linked publications0
Agent typeDrug (Small molecule)
Development stage (any indication)Approved
Mechanism / classNot recorded
Data sourcesDGIdb
Linked via biomarker / targetCTLA4
How the evidence score is calculated
  • Each registered trial scores by status (recruiting / active / enrolling 3, completed 2.5, not yet recruiting 2, unknown 1, terminated / withdrawn / suspended 0.5) plus a phase bonus (phase 3-4 +2, phase 2 +1, phase 1 +0.5). The trial component is capped at 30.
  • Each literature item scores by design (Cochrane review 5, meta-analysis 4, systematic review 3, RCT 3, clinical trial publication 2, curated reference 1.5, other PubMed record 1). The literature component is capped at 30.
  • The existing evidence tier adds 15 (A / Strong), 10 (B / Moderate), 5 (C / Preliminary) or 0 (D / Anecdotal).
  • Agents approved for any indication (max clinical phase 4) add 5, because an approved agent has an established safety profile that lowers the barrier to repurposing trials.
  • The score ranks what has been studied, not what works. It does not read effect sizes or directions of effect.

Registered clinical trials

NCT IDTitleStatusPhaseEnrolment
NCT00006055Autologous Peripheral Blood Stem Cell Transplantation in Patients With Life Threatening Autoimmune Diseases
2000
status unknownNot applicable10

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Published literature

No publication is linked to this pair yet.

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Mechanism and notes

No mechanism of action is recorded for this pair in the source databases.

OSMF's existing evidence tier for this pair is A (Strong), derived from the strength of the disease association recorded in DGIdb, in this case via the biomarker or target CTLA4. The tier describes how well the drug-disease link is documented, not how well the drug works.

Frequently asked questions

Is Anti-Thymocyte Globulin approved for Immune Thrombocytopaenia (ITP)?

Anti-Thymocyte Globulin has reached the approved stage (maximum clinical phase 4) for at least one indication, so its use in Immune Thrombocytopaenia (ITP) would be drug repurposing rather than first-in-human development. This does not mean it is approved for Immune Thrombocytopaenia (ITP). Approval status for the specific indication should always be confirmed with the relevant regulator and prescribing information.

Is Anti-Thymocyte Globulin in clinical trials for Immune Thrombocytopaenia (ITP)?

ClinicalTrials.gov lists 1 registered trial linking Anti-Thymocyte Globulin to Immune Thrombocytopaenia (ITP): 1 is terminated, withdrawn, suspended or of unknown status. None of the registered studies carries a drug-development phase label, which is typical for behavioural, device and supplement protocols. It plans or enrolled 10 participants. Registered activity dates to 2000.

What does the evidence show for Anti-Thymocyte Globulin in Immune Thrombocytopaenia (ITP)?

Trials of Anti-Thymocyte Globulin in Immune Thrombocytopaenia (ITP) are registered but none has completed, so there is no outcome evidence from those studies yet; the record is a signal of research interest. OSMF's existing evidence tier for this pair is A (Strong), derived from the strength of the disease association recorded in DGIdb, in this case via the biomarker or target CTLA4. The tier describes how well the drug-disease link is documented, not how well the drug works.

Cite this page

Open Source Medicine Foundation. Anti-Thymocyte Globulin for Immune Thrombocytopaenia (ITP): evidence, trials and status. OSMF Research Tracker. Updated 2026-07-06. https://research.opensourcemed.info/pairs/autoimmune-thrombocytopenic-purpura/anti-thymocyte-globulin.html

Data: ClinicalTrials.gov, PubMed, Open Targets, ChEMBL, DGIdb and the OSMF therapeutic agent database. Last updated 2026-07-06. Page built 2026-10-07.

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This is a research map, not treatment advice. Evidence tiers and scores summarise what has been studied, not whether a treatment works or is safe for you.