Clinical trial · Interventional
Ph 2 Open Label Study of GC4419 to Reduce SOM Associated With Chemoradiotherapy for Head and Neck Cancer
An Open Label Multi-Center Study of the Effects of GC4419 When Administered to Reduce the Incidence and Severity of Severe Oral Mucositis Associated With Chemo RT for Locally Advanced, Non-Metastatic Head and Neck Cancer
NCT04529850CI-TRIAL-00060347completedPhase 2Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
GTI-4419-202 is a Phase 2 open-label study of the effects of GC4419 (IV) when administered in combination with IMRT and cisplatin to up to subjects with head and neck cancer, who are at high risk for Severe Oral Mucositis (SOM)
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Head and Neck Cancer | Malignant Head and Neck Neoplasm | ALIAS | 0.90 |
| Oral Mucositis | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cisplatin | Drug | Cisplatin | ALIAS |
| Drug: GC4419 | Drug | — | UNRESOLVED |
| Intensity-modulated radiation therapy (IMRT) | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Open Label Active Arm
- description
- 90mg GC4419 by IV
- interventionNames
- Drug: Drug: GC4419
- Radiation: Intensity-modulated radiation therapy (IMRT)
- Drug: Cisplatin
Primary outcomes (1)
- measure
- Incidence of Treatment Emergent AE's
- timeFrame
- First dose of study medication through the 30 days following the last dose of IMRT, GC4419, or cisplatin (whichever occurs last) which is estimated to be 11 weeks
- description
- Number of Subjects with at Least One Treatment Emergent Adverse Event (TEAE)
Secondary outcomes (1)
- measure
- Cumulative Incidence of Severe OM
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Pathologically-confirmed diagnosis of locally advanced squamous cell carcinoma of the head and neck that will be treated with cisplatin plus concurrent IMRT. 2. Treatment plan to receive a continuous course of IMRT delivered as single daily fractions of 2.0 to 2.2 Gy with a cumulative radiation dose of 60-72 Gy. 3. Patients who have had prior surgery may be eligible, 4. Treatment plan to receive standard cisplatin monotherapy administered either every three weeks (100 mg/m2 for 3 doses) or weekly (40 mg/m2 for 6-7 doses). 5. Age 18 years or older 6. ECOG performance status ≤ 2 7. Adequate hematologic function 8. Adequate renal and liver function Alkaline phosphatase ≤ 2.5 ULN Exclusion Criteria: 1. Metastatic disease 2. Prior radiotherapy to the region of the study cancer or adjacent anatomical sites 3. Prior induction chemotherapy or plans for chemotherapy to be administered only sequentially with IMRT 4. Planned concurrent chemotherapy other than single agent cisplatin 5. Receiving any approved or investigational anti-cancer agent 6. Concurrent participation in another interventional clinical study 7. Inability to eat soft solid food at baseline for reasons other than mouth soreness after surgery or dental procedures 8. Complete reliance on parenteral or gastrointestinal tube-delivered nutrition at baseline 9. Malignant tumors other than head and neck cancer (HNC) within the last 5 years 10. Active infectious disease excluding oral candidiasis 11. Presence of oral mucositis at baseline. 12. Known history of human immunodeficiency virus (HIV) or active hepatitis B/C 13. Female patients who are pregnant or breastfeeding 14. Known allergies or intolerance to cisplatin and similar platinum-containing compounds 15. Requirement for concurrent treatment with nitrates or other drugs that may, in the judgment of the treating Investigator, create a risk for a precipitous decrease in blood pressure.
References
Publications (0)
Data not yet available
No reference posted for this study.