Osilodrostat Phosphate

Evidence Level: L5 Predicted Indications: 50

Quick Overview

Item Value
Drug Name Osilodrostat Phosphate
DrugBank ID DB11837
Brand Names (EU) Isturisa
Evidence Level L5
Predicted Indications 50
Top Prediction Score 98.19%

Approved Indication (EMA)

Isturisa is indicated for the treatment of endogenous Cushing’s syndrome in adults.


Predicted New Indications

TxGNN model predictions for potential drug repurposing:

Rank Indication Score Source
1 familial generalized lentiginosis 98.19% DL
2 acromelanosis 98.05% DL
3 congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome 98.05% DL
4 gastrocutaneous syndrome 97.96% DL
5 leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome 97.88% DL
6 Moynahan syndrome 97.77% DL
7 rhabdoid tumor 97.76% DL
8 X-linked lymphoproliferative disease due to SH2D1A deficiency 97.68% DL
9 osteopathia striata-pigmentary dermopathy-white forelock syndrome 97.66% DL
10 peripheral nerve schwannoma 97.51% DL
11 schwannoma of twelfth cranial nerve 97.40% DL
12 sympathetic neurilemmoma 97.37% DL
13 microcystic/reticular schwannoma 97.33% DL
14 trigeminal schwannoma 97.33% DL
15 ACTH-dependent Cushing syndrome 97.28% DL
16 A20 haploinsufficiency 97.20% DL
17 benign neoplasm of adrenal gland 97.12% DL
18 immune dysregulation with inflammatory bowel disease 96.96% DL
19 Steel syndrome 96.84% DL
20 hemophagocytic syndrome associated with an infection 96.47% DL

Showing top 20 of 50 predictions.


About TxGNN Predictions

Prediction Sources

Source Description
KG Knowledge Graph - Network topology-based associations
DL Deep Learning - Neural network score prediction

Evidence Levels

Level Definition
L1 Multiple Phase 3 RCTs / Systematic Reviews
L2 Single RCT or multiple Phase 2 trials
L3 Observational studies / Large case series
L4 Preclinical / Mechanistic / Case reports
L5 AI prediction only (current)

Clinical Validation Needed

Research Use Only: These predictions are computational hypotheses that require clinical validation. They should NOT be used for clinical decision-making.

Next Steps for Validation

  1. Literature Review: Search PubMed for existing evidence
  2. Clinical Trial Search: Check ClinicalTrials.gov for ongoing studies
  3. Mechanistic Analysis: Evaluate biological plausibility
  4. Preclinical Studies: Conduct in vitro/in vivo validation
  5. Clinical Trials: Design and conduct human studies

Data Access


Citation

If using this data, please cite:

@article{huang2023txgnn,
  title={A foundation model for clinician-centered drug repurposing},
  author={Huang, Kexin and others},
  journal={Nature Medicine},
  year={2023},
  doi={10.1038/s41591-023-02233-x}
}

Disclaimer: This report is for research purposes only and does not constitute medical advice. Drug repurposing predictions require rigorous clinical validation before any therapeutic application.

Copyright © 2026 EuTxGNN Project. For research purposes only. Not medical advice.