Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06448026 · ClinicalTrials.gov registry record · Phase 2

Cemiplimab and Cetuximab Prior Salvage Surgery in Patients With Recurrent Oral Cavity Squamous Cell Carcinoma (OCSCC).

A Phase 2 study of Locally Recurrent Oral Cavity Squamous Cell Carcinoma, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
Phase 2
Development phase
17
Enrollment target
1
Study location

NCT06448026: Recruiting Phase 2 study of Locally Recurrent Oral Cavity Squamous Cell Carcinoma, sponsored by M.D. Anderson Cancer Center.

NCT06448026 is a Phase 2 study of Locally Recurrent Oral Cavity Squamous Cell Carcinoma that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 17 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06448026, a Phase 2 study of Locally Recurrent Oral Cavity Squamous Cell Carcinoma, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

RECRUITING
Registry status
Phase 2
Development phase
17 participants
Enrollment target
1
Study location

Study Summary

To learn if giving cemiplimab and cetuximab before salvage surgery can help to control recurrent oral cavity squamous cell carcinoma.

Primary Outcome

Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0

Interventions

  • DRUG Cemiplimab
  • DRUG Cetuximab

Study Locations (1)

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2024-11-21
Est. Completion 2027-05-15
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What NCT06448026 shows while recruiting

NCT06448026 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower).

The record links to 1 condition, with Locally Recurrent Oral Cavity Squamous Cell Carcinoma appearing as the primary indexed condition, and to 2 interventions - of which Cemiplimab is the first listed.

NCT06448026 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT06448026 about?

NCT06448026 is a clinical study titled "Cemiplimab and Cetuximab Prior Salvage Surgery in Patients With Recurrent Oral Cavity Squamous Cell Carcinoma (OCSCC).". To learn if giving cemiplimab and cetuximab before salvage surgery can help to control recurrent oral cavity squamous cell carcinoma.

What is the current status of trial NCT06448026?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 17 participants. The study started on 2024-11-21. Estimated completion is 2027-05-15.

What conditions does trial NCT06448026 study?

This clinical trial studies the following conditions: Locally Recurrent Oral Cavity Squamous Cell Carcinoma.

What interventions are being tested in trial NCT06448026?

The interventions under investigation include: Cemiplimab (DRUG), Cetuximab (DRUG).

Who is sponsoring clinical trial NCT06448026?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06448026 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Locally Recurrent Oral Cavity Squamous Cell Carcinoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06448026's enrollment target sits among peer trials

17 1904th of 2000 higher than 93 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02090140 · 17 participants · NA

    Microfracture Versus Adipose Derived Stem Cells for the Treatment of Articular Cartilage Defects

  • NCT03317860 · 17 participants · NA

    Improving Measurement and Treatment of Post-stroke Neglect

  • NCT04356469 · 17 participants · Phase 2

    TCR Alpha Beta T-cell Depleted Haploidentical HCT in the Treatment of Non-Malignant Hematological Disorders in Children

  • NCT04414046 · 17 participants · Phase 2

    TCR Alpha Beta T-cell Depleted Haploidentical HCT in the Treatment of Primary Immunodeficiency and Inherited Metabolic Disorders in Children

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06448026, the US trial registry maintained by the National Library of Medicine. NCT06448026 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.