A Dose Escalation Study of HFB301001 in Adult Patients with Advanced Solid Tumors

Overview

Información sobre este estudio

The purpose of this study is to characterize the safety and tolerability of single agent HFB301001 and to determine recommended dose expansino (RDE(s) and a recommended Phase 2 dose (RP2D).

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

- Previously received the following lines of systemic therapy for the
advanced/metastatic disease:

- Soft tissue sarcoma: at least 1 line of therapy

- Renal cell carcinoma: at least 2 lines of therapy;

- Uterine carcinosarcoma: at least 1 line of therapy;

- Hepatocellular carcinoma: at least 1 line of therapy

- Head and neck squamous cell carcinoma: at least 2 lines of therapy

- Suitable site to biopsy at pre-treatment and on-treatment

- Measurable disease as determined by Response Evaluation Criteria in Solid Tumors
(RECIST) 1.1 and immune-RECIST (iRECIST)

- Eastern Cooperative Oncology Group performance status of 0 or 1.

Exclusion Criteria:

- Systemic anti-cancer therapy within 2 weeks prior to start of study drug.

- For soft tissue sarcoma and uterine carcinosarcoma patients only: prior immune therapy

- Therapeutic radiation therapy within the past 2 weeks

- Prior exposure to agents targeting the OX40 receptor;

- Active autoimmune disease requiring systemic treatment in the previous 2 years;

- Systemic steroid therapy (>10 mg/day of prednisone or equivalent) or any immune
suppressive therapy.

- Persisting toxicity of >Grade 1 relating to prior anti cancer therapy with the
following exceptions:

- All grades of alopecia are acceptable;

- Endocrine dysfunction on replacement therapy is acceptable.

- Severe or unstable medical condition, including uncontrolled diabetes, coagulopathy,
or unstable psychiatric condition;

- Major surgery within 2 weeks of the first dose of study drug;

- History or presence of drug or non-drug induced interstitial lung disease or
pneumonitis ≥Grade 2;

- History of allergic reactions attributed to compounds of similar chemical or biologic
composition to monoclonal antibodies or any excipient of HFB301001;

- Known active malignancy, with the exception of the specific cancer under investigation
in this trial, that required treatment within the previous 2 years.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Eligibility last updated 1/19/23. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Konstantinos Leventakos, M.D., Ph.D.

Cerrado para la inscripción

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

Scottsdale/Phoenix, Ariz.

Investigador principal de Mayo Clinic

Mitesh Borad, M.D.

Cerrado para la inscripción

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Hani Babiker, M.D.

Cerrado para la inscripción

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

More information

Publicaciones

Publications are currently not available
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