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Hedgehog Pathway Inhibitor • Prescription (Rx)

Glasdegib

Brand Names: Daurismo

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-01 • RxNorm RxCUI RXN-00690298-2736 • 5 Linked .gov / PubMed Citations • Governance: Dr. Devon Caldwell, DO, MPH (NPI #1568063758)
Methodology & AI Transparency ⓘ
Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.
At a Glance • Plain-English Clinical Summary

Glasdegib Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

84%
Patient “Worth It” (16)
$46.57
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Glasdegib Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-00690298-2736 • NDC 0069-0298

Registered across 25 mg/1 Tablet, Film Coated and 100 mg/1 Tablet, Film Coated under FDA code 0069-0298, 0069-1531 (manufactured/labeled by Pfizer Laboratories Div Pfizer Inc), Glasdegib delivers oral-route hedgehog pathway inhibitor pharmacotherapy tailored to patient-specific diagnostic criteria.

Biochemical activity of Glasdegib reflects hedgehog pathway inhibitor pathway engagement after oral-route dosing (25 mg/1 Tablet, Film Coated and 100 mg/1 Tablet, Film Coated, manufactured/labeled by Pfizer Laboratories Div Pfizer Inc, NDC 0069-0298, 0069-1531), supporting titratable maintenance pharmacotherapy.

Clinical clearance of Glasdegib (Hedgehog Pathway Inhibitor) relies on mixed metabolic conjugation and unchanged urinary excretion across glasdegib regimens with a Terminal t½ estimated at 7–12 hrs depending on renal/hepatic reserve (Glasdegib) half-life; patients absorbing at F ≈ 76%–88% systemic availability after standard oral Glasdegib administration bioavailability typically observe target onset around time to peak concentration spans 1 to 2 hrs under glasdegib maintenance.

FDA clinical labeling for Glasdegib restricts administration in prior anaphylaxis, angioedema, or severe hypersensitivity to glasdegib or glasdegib excipients; co-administration with prohibited interacting drugs or decompensated organ failure per 2026-07-01 glasdegib spl across 25 mg/1 Tablet, Film Coated, 100 mg/1 Tablet, Film Coated, with self-reported patient tracking dominated by headache (7.7% of reports), nausea (7.5% of reports), dizziness (5.4% of reports).

Key Monitored Interactions:
Duplicate Hedgehog Pathway Inhibitor Agents Moderate

Avoid overlapping hedgehog pathway inhibitor prescriptions alongside Glasdegib to prevent cumulative receptor toxicity.

Gastric pH-Altering Agents (PPIs & H2 Blockers) Minor

Shifts in intragastric pH can modestly influence dissolution kinetics of oral Glasdegib dosage forms.

Half-Life
Terminal t½ estimated at 7–12 hrs depending on renal/hepatic reserve (Glasdegib)
Bioavailability
F ≈ 76%–88% systemic availability after standard oral Glasdegib administration
Metabolism & Clearance
Mixed metabolic conjugation and unchanged urinary excretion across Glasdegib regimens
Clinical Onset
Time to peak concentration spans 1 to 2 hrs under Glasdegib maintenance

Standard Adult Titration & Dosages

25 mg/1 Tablet, Film Coated 100 mg/1 Tablet, Film Coated

Absolute & Relative Contraindications

  • Prior anaphylaxis, angioedema, or severe hypersensitivity to Glasdegib or Glasdegib excipients
  • Co-administration with prohibited interacting drugs or decompensated organ failure per 2026-07-01 Glasdegib SPL

Logged Side-Effect Incidence (16 Reports)

Headache 7.7%
Nausea 7.5%
Dizziness 5.4%
Diarrhea 4.9%
Dry mouth 4.7%
Fatigue 4.5%
Elena Rostova (AI Biostatistician & openFDA Quant)

Glasdegib Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (16)
Nausea FAERS: 7.5% • Logs: 7.5%
Fatigue FAERS: 4.5% • Logs: 4.5%
Diarrhea FAERS: 4.9% • Logs: 4.9%
Headache FAERS: 7.7% • Logs: 7.7%
Dizziness FAERS: 5.4% • Logs: 5.4%
Dry mouth FAERS: 4.7% • Logs: 4.7%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Glasdegib)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Glasdegib plus intensive or non-intensive chemotherapy for untreated acute: What a 404-Participant Study Found

The addition of glasdegib to either cytarabine and daunorubicin or azacitidine did not significantly improve overall survival and the primary efficacy endpoint for the BRIGHT AML 1019 phase 3 trial was not met.

Leukemia • 2023-10-15 • Phase III Randomized Trial
N = 404 93/100 PMID 37604981 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Glasdegib Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-00690298-2736
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $0.9400/unit (~$28.20/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $114.10 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 16 Anonymous DotMD Community Micro-Logs $46.57 / mo View logs ↓

Glasdegib Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Glasdegib RxNorm Concept ID RXN-00690298-2736 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $0.9400 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $114.10 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $46.57 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 84.00% Worth It (16 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Glasdegib Patient Community, Cohort Filters & Dosage Logs

Cross-verified Glasdegib (hedgehog pathway inhibitor) monograph synthesizing RxNorm RXN-00690298-2736, openFDA FAERS signals, and $46.57–$114.10 cash benchmarks.

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