Overview

Randomized Pre-surgical Window-of-Opportunity Trial of TTI-101 in Patients With Stage II-IV Resectable HPV-negative Squamous Cell Carcinoma of the Head and Neck

Status:
Not yet recruiting
Trial end date:
2025-02-01
Target enrollment:
0
Participant gender:
All
Summary
To learn if TTI-101 can reduce the growth of HPV-negative squamous cell carcinomas of the head and neck when given before standard of care surgery.
Phase:
Early Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborators:
National Institutes of Health (NIH)
Tvardi Therapeutics, Inc
Criteria
Inclusion Criteria:

Patients must meet the following criteria for study entry:

- Biopsy-proven primary Stage II-IV squamous cell carcinoma of the head and neck

- For oropharyngeal cancer patients: HPV-negative by p16 and/or direct high-risk HPV
assessment

- Surgical resection must be planned as primary therapy with or without adjuvant
radiation therapy.

- Signed Informed Consent Form (ICF).

- Ability and willingness to comply with the requirements of the study protocol.

- Ability to swallow study drug.

- Age years of 18 years.

- Measurable disease per RECIST v1.1 (see Appendix 2) and/or per direct clinical
measurements.

- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1 (see Appendix
4)

- Adequate hematologic and hepatorenal function, defined by the following laboratory
results obtained within 4 weeks prior to study entry:

- ANC 1500 cells/L

- Platelet count 100,000/L;

- Hemoglobin 9.0 g/dL

- Total bilirubin 1.5 upper limit of normal (ULN) with the following exception:

Patients with known Gilbert disease who have serum bilirubin level 3 ULN may be enrolled.

- AST and ALT 2.5 ULN

- Alkaline phosphatase 2.5 ULN

- Serum creatinine clearance ≥60 mL/min, measured or calculated per institutional
standard protocol

• INR and aPTT 1.5 ULN

- This applies only to patients who do not receive therapeutic anticoagulation; patients
receiving therapeutic anticoagulation (such as low-molecular-weight heparin or
warfarin) should be on a stable dose.

- No evidence of distant metastases.

- A male participant must agree to use contraception as detailed in Appendix 3 of
this protocol during the treatment period and for at least 90 days after the last
dose of study treatment and refrain from donating sperm during this period.

- A female participant is eligible to participate if she is not pregnant, not
breastfeeding, and at least one of the following conditions applies:

- Not a woman of childbearing potential (WOCBP) as defined in Appendix 3 OR

- A WOCBP who agrees to follow the contraceptive guidance in Appendix 3 during the
treatment period and for at least 90 days after the last dose of study treatment.

Exclusion Criteria:

Patients who meet any of the following criteria will be excluded from study entry.

General Exclusion Criteria:

- Any prior systemic or radiotherapy within the last 4 months directed towards the
squamous cell carcinoma of the head and neck that is to be resected as part of SOC
therapy.

- Standard of care anticancer therapy, including chemotherapy, hormonal therapy, or
radiotherapy, for concurrent malignancy or unresected squamous cell carcinoma of the
head and neck within 3 weeks prior to initiation of study treatment.

- AEs from prior anticancer therapy that have not resolved to Grade 1 except for
alopecia, Grade 2 neuropathy or endocrine-related AEs Grade ≤2 requiring treatment or
hormone replacement are eligible

- Pregnancy, lactation, or breastfeeding

- Inability to comply with study and follow-up procedures

- Has a known active Hepatitis B (defined as Hepatitis B RNA detected) or known active
Hepatitis C virus (defined as HCV RNA is detected) infection, or known active HIV
(defined as HIV RNA is detected) infection.

- Active tuberculosis

- Severe infections within 4 weeks prior to treatment, including but not limited to
hospitalization for complications of infection, bacteremia, or severe pneumonia

- Signs or symptoms of infection as determined by the treating team within 2 weeks prior
to treatment

- Major surgical procedure within 28 days prior to treatment

- Has received a live vaccine or live-attenuated vaccine within 30 days prior to the
first dose of study drug. Administration of killed or mRNA vaccines is allowed.

- Has a known additional malignancy that is progressing or has required active treatment
within the past 3 years. Participants with basal cell carcinoma of the skin, squamous
cell carcinoma of the skin, well-differentiated thyroid cancer, or carcinoma in situ
that have undergone potentially curative therapy are not excluded.

- History of significantly impaired cardiac function such as unstable angina pectoris,
congestive heart failure with New York Heart Association (NYHA) class III or IV,
myocardial infarction within the last 12 months prior to trial entry; signs of
pericardial effusion, serious arrhythmia (including QTc prolongation of >470 ms and/or
pacemaker) or prior diagnosis of congenital long QT syndrome or left ventricular
ejection fraction <50% on echocardiogram.

- History of cerebral vascular accident or stroke within the previous 2 years.

- Uncontrolled hypertension (>160/100mm Hg).

- History of Grade 3 or 4 allergic reactions attributed to compounds of similar
chemicalor biologic composition as TTI-101 (hydroxyl-naphthalene sulfonamides).

- Patients with prior allogeneic bone marrow transplantation or prior solid organ
transplantation

- Previous treatment of the current malignancy with a STAT inhibitor.

- Any other diseases, metabolic dysfunction, physical examination finding, or clinical
laboratory finding giving reasonable suspicion of a disease or condition that
contraindicates the use of an investigational drug or that may affect the
interpretation of the results or render the patient at high risk from treatment
complications

Medication-Related Exclusion Criteria:

- Bisphosphonate therapy for symptomatic hypercalcemia

- Use of bisphosphonate therapy for other reasons (e.g., osteoporosis) is allowed.

- Received oral or IV antibiotics within 2 weeks prior to treatment

- Patients receiving prophylactic antibiotics (e.g., for prevention of a urinary tract
infection or chronic obstructive pulmonary disease) are eligible.

- Treatment with an investigational agent (not standard of care) within 3 weeks prior to
treatment (or within five halflives of the investigational product, whichever is
longer)

- Treatment with systemic immunosuppressive medications (including but not limited to
prednisone, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor
necrosis factor [anti-TNF] agents) within 2 weeks prior to treatment

- Patients who have received acute, low dose, systemic immunosuppressant
medications (e.g., a one-time dose of dexamethasone for nausea) may be enrolled.

- The use of inhaled corticosteroids and mineralocorticoids (e.g., fludrocortisone)
for patients with orthostatic hypotension or adrenocortical insufficiency is
allowed.