A Phase 1 Study Evaluating the Safety, PK, and Clinical Effects of PT-112 in Subjects With Advanced Solid Tumors

Overview

Información sobre este estudio

The purpose of this study is to determine the maximum tolerated dose, and evaluate its safety, tolerability, preliminary clinical effects, and drug/body interactions.

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.

Key Inclusion Criteria:

- Pathologically confirmed advanced solid tumor for which standard therapy proven to
provide clinical benefit does not exist or is no longer effective.

- Eastern Collaborative Oncology Group (ECOG) Performance Status of 0-1.

- Progressive disease, either measurable on physical examination or imaging by Response
Evaluation Criteria in Solid Tumors (RECIST v1.1) or PCWG3 or by informative tumor
marker(s).

- Adequate organ function based on laboratory values.

- If there is a known history of brain metastases, either treated or untreated, the
disease must be stable.

- Willing and able to provide written Informed Consent and comply with the requirements
of the study.

Key Exclusion Criteria:

- Any cytotoxic chemotherapy within 21 days prior to initiation of study drug.

- Any immunomodulatory drug therapy, anti-neoplastic hormonal therapy, immunosuppressive
therapy, corticosteroids, or growth factor treatment within 14 days prior to
initiation of study drug.

- Presence of an acute or chronic toxicity of prior chemotherapy, that has not resolved
to ≤Grade 1, as determined by CTCAE v 4.0.

- Receipt of more than 3 prior regimens of cytotoxic chemotherapy for metastatic
disease.

- Bone marrow reserve which is not adequate for participation in this trial.

- Radiotherapy within 28 days prior to baseline.

- Fraction of radiotherapy to >25 % of bone marrow.

- Major surgery within 28 days prior to initiation of study drug.

- Active bacterial, viral, or fungal infection requiring systemic therapy.

- Known human immunodeficiency virus or acquired immunodeficiency syndrome related
illness.

- Clinically significant hearing impairment, as judged by the Principal Investigator.

- Uncontrolled cardiovascular abnormalities.

- Previous malignancy, except for non-squamous-cell carcinoma of skin or carcinoma
in-situ of the uterine cervix, unless the tumor was treated with curative intent more
than 2 years prior to study entry.

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

Eligibility last updated 9/7/22. 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

Brian Costello, M.D.

Cerrado para la inscripción

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Roxana Dronca, M.D.

Cerrado para la inscripción

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

Scottsdale/Phoenix, Ariz.

Investigador principal de Mayo Clinic

Irbaz Riaz, M.B.B.S., M.S.

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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CLS-20236303

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