Study to Evaluate the Safety and Efficacy of Oral NRC-2694-A in Combination With Paclitaxel in Patients With Recurrent and/or Metastatic Head and Neck Squamous Cell Carcinoma, Who Progressed on or After Immune Checkpoint Inhibitor Therapy

Launched by NATCO PHARMA LTD. · Mar 8, 2022

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called NRC-2694-A combined with a standard chemotherapy medication, paclitaxel, for patients with advanced head and neck cancer that has come back or spread after previous treatments. The goal is to see if this combination is safe and effective for patients whose cancer has progressed despite receiving immune checkpoint inhibitors, which are a type of cancer treatment that helps the immune system fight cancer. The trial will include about 46 participants, and researchers hope to find that at least half of them will benefit from this new treatment.

To participate in the trial, patients must be at least 18 years old, have a specific type of head and neck cancer that cannot be surgically removed, and have shown signs of cancer progression after prior treatments. Eligible participants will need to provide consent and meet certain health requirements, such as having a good performance status and normal blood counts. Throughout the study, participants will have regular check-ups to monitor their health and response to the treatment. This trial is important as it may lead to new options for patients who have limited treatment choices left.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Is willing and capable of understanding the written informed consent, provides signed and witnessed written informed consent, and agrees to comply with protocol requirements.
• • Is male or female aged 18 years or older at the time of consent.
• • Has histologically confirmed unresectable R/M HNSCC (oral cavity, oropharynx, hypopharynx, and larynx).
• • Has documented progressive disease assessed by the principal investigator according to RECIST v1.1.
• • Has a measurable lesion per RECIST v1.1.
• • Has ECOG performance status score of ≤2.
• • Must have progressed during or after receiving ICI therapy, such as pembrolizumab or nivolumab. Patients with prior immune-mediated reactions due to ICI therapies (eg, pembrolizumab or nivolumab) and who had recovered prior to study entry will also be eligible.
• • Female patients of childbearing potential should have a negative urine test before enrollment. If the urine pregnancy test is positive or gives equivocal results, a serum pregnancy will be required for confirmation.
• • Patients of reproductive age must use acceptable methods of contraception throughout the study period and for 30 days following the last dose of investigational product (see protocol for further guidance).
• • During screening and at subsequent visits, the investigator should ensure adequate bone marrow reserve (neutrophil count ≥1500/mm3, platelet count ≥100,000/mm3, and hemoglobin level 8.0 g/dL), renal function (creatinine clearance ≥30 mL/min calculated by Cockcroft-Gault formula), liver function (total bilirubin level ≤1.5 × ULN \[except patients with documented Gilbert's syndrome\] and serum transaminase levels ≤2.5 × ULN or ≤5 × ULN for liver metastasis and/or obstructive jaundice).
• • Must have completed a duration of at least two weeks after stopping ICI therapy/investigational therapy/salvage therapy and must have recovered to grade ≤1 from all toxicities due to such therapies.
• Exclusion Criteria:
• • Has cardiac, hepatic, endocrine, pulmonary, or autoimmune disease, interstitial lung disease, renal or psychiatric disorders, not controlled with therapy corresponding to the illness or a condition that contraindicates the use of a taxane or an EGFR inhibitor.
• • Has Cirrhosis of liver at a level of Child-Pugh B (or worse).
• • Has uncontrolled brain metastases. Patients are allowed if brain metastasis has been previously treated with surgery, whole brain irradiation, and/or stereotactic radiosurgery and are considered controlled (controlled by the dose ≤10 mg/day of prednisone or equivalent) at the time of the first dose of investigational product. Radiological evaluation of brain metastasis will be performed only if the patient has symptoms. For asymptomatic patients, brain imaging during screening is not required.
• • Has baseline prolongation of QT/QTc interval (eg, repeated demonstration of a QTc interval \>480 milliseconds \[CTCAE Grade 1\] using Fredericia's QT correction formula).
• • Has a history of additional risk factors for Torsade de pointes (eg, heart failure, hypokalemia, family history of long QT syndrome).
• • Has had prior cetuximab therapy for recurrent or metastatic disease. Note that cetuximab used concomitantly with radiotherapy or as an induction therapy is acceptable
• • Has received any other EGFR-targeted therapies for recurrent or metastatic disease.
• • Currently participating in any clinical trial or receiving investigational therapy on expanded access or compassionate basis.
• • Has nasopharyngeal carcinomas or salivary gland cancers.
• • Female patient who tested positive for pregnancy.
• • Female patient who is breastfeeding or planning to become pregnant, or male patient planning to father a child within the duration of the study.
• • Has tested positive for HIV, HBsAg, HCV antibody, or HCV RNA at screening. However, patients who test positive for HCV antibody, but negative for HCV RNA, will be allowed. In addition, patients with controlled HIV, chronic HBV on suppressive antiviral therapy, or a history of HCV infection status post-curative antiviral treatment with an HCV viral load below limit of quantification are permitted to participate (DHHS 2020).
• • Has active infection requiring intravenous anti-infective therapy within 7 days prior to Day 1 Cycle 1 or is febrile due to infection.
• • Has had major surgery within 4 weeks prior to screening.
• • Administered a live attenuated vaccine within 4 weeks prior to Day 1 Cycle 1 or anticipation that such a live attenuated vaccine will be required during the study.
• • Has known or suspected hypersensitivity to any components of the formulation used for this investigational product.
• • Has concurrent disease or any clinically significant abnormality following the investigator's review of the screening physical examination findings, 12-lead ECG results, and clinical laboratory tests, which in the judgment of the investigator would interfere with the patient's participation in this study or evaluation of study results.
• • Unable to come for study visits per schedule.
• • Has current drug or alcohol abuse.
• • Has received prior treatment with paclitaxel or docetaxel or any other drugs with taxane like mode of action for recurrent or metastatic or recurrent HNSCC. However, prior paclitaxel or docetaxel or any other drugs with taxane like mode of action as a component of a curatively-intended multimodality treatment for locally advanced HNSCC is permitted.