NCT05683470

Brief Summary

This is an expanded access treatment protocol designed to provide access of RBS2418 to a single patient with pancreatic cancer.

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 26, 2022

Completed
18 days until next milestone

First Posted

Study publicly available on registry

January 13, 2023

Completed
Last Updated

February 21, 2024

Status Verified

February 1, 2024

First QC Date

December 26, 2022

Last Update Submit

February 18, 2024

Conditions

Interventions

RBS2418 will be administered orally at 200 mg two times per day (BID).

Eligibility Criteria

Sexfemale
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • The patient is willing and able to provide informed consent. Only the patient for whom this clinical study/experimental treatment was designed will be given the investigational drug under the treatment of the PI. No other patient is authorized to participate in or to receive treatment under this treatment protocol.

You may not qualify if:

  • Not applicable

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Bertrand Tuan, MD

    Pacific Hematology and Oncology Associates

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
expanded access
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 26, 2022

First Posted

January 13, 2023

Last Updated

February 21, 2024

Record last verified: 2024-02