Expanded Access Use of DKN-01 for the Treatment of Advanced Solid Tumors

Sponsor
Leap Therapeutics, Inc. (Industry)
Overall Status
Available
CT.gov ID
NCT04681248
Collaborator
(none)
4

Study Details

Study Description

Brief Summary

An Expanded Access Protocol for use of DKN-01 for the treatment of advanced solid tumors.

Detailed Description

This is a intermediate-size Expanded Access Protocol (EAP). Patients who were receiving DKN-01 in a parent study at the time of completion of the parent study, and are, in the opinion of the Investigator and Sponsor, suitable candidates for continued study drug treatment are eligible for participation in the current EAP. In this EAP, all patients will receive DKN-01 at the same dose and schedule as at the time of completion of the parent study. Furthermore, patients who received DKN-01 in combination in the parent study will continue to receive the same combination agent at the same dose and schedule in the EAP.

Study Design

Study Type:
Expanded Access
Official Title:
Expanded Access Use of DKN-01 for the Treatment of Advanced Solid Tumors

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Must be ≥18 years of age

    • Receiving DKN-01 in a parent study and, in the opinion of the Investigator and Leap, is a suitable candidate for continued study drug treatment at the completion of the parent study

    • In the Investigator's opinion, demonstrated acceptable tolerability of study drug

    • In the Investigator's opinion, is receiving clinical benefit from treatment with DKN-01, either as monotherapy or in combination with another treatment in the parent study

    • In the Investigator's opinion, demonstrated acceptable compliance with study drug and the study procedures in the parent study and is willing and able to comply with all procedures in the current study.

    • After consultation with the Medical Monitor, DKN-01 may be continued for a patient who has met the criteria for Progressive Disease (PD) but, in the Investigator's opinion, is receiving clinical benefit

    • For men and women of child-producing potential, the use of effective contraceptive methods during the study and for 6 months following the last dose of study drug

    • Signed informed consent must be obtained prior to the initiation of any study-required procedures.

    Exclusion Criteria:
    Patients with any of the following characteristics will be ineligible for study entry:
    • Any unresolved toxicity that meets the study treatment discontinuation or study withdrawal criteria from the parent study at the time of transition to this study

    • Permanent discontinuation of DKN-01 in the parent study due to toxicity

    • Any serious and/or unstable pre-existing medical, psychiatric disorder or other conditions at the time of transition to this study that could interfere with subject's safety, obtaining informed consent or compliance to the study procedures, in the opinion of the investigator or Leap Medical Monitor or designee

    • Patient has experienced Progressive Disease (PD) that, in the opinion of the Investigator, precludes further study treatment.

    • Patient requires use of a prohibited concomitant medication or therapy listed in the parent study

    • Females who are breastfeeding or pregnant, and females and males planning a pregnancy

    • Current evidence of any condition (including medical, psychiatric or substance abuse disorder), therapy, or laboratory abnormality that might interfere with the patient's participation or is not in the best interest of the patient to participate, in the opinion of the treating Investigator

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Alabama Birmingham Alabama United States 35294
    2 Cedars Sinai Medical Care Foundation Los Angeles California United States 90025
    3 Northwestern University Chicago Illinois United States 60611
    4 University of Wisconsin Madison Wisconsin United States 53715

    Sponsors and Collaborators

    • Leap Therapeutics, Inc.

    Investigators

    • Study Director: Cyndi Sirard, MD, Leap Therapeutics

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Leap Therapeutics, Inc.
    ClinicalTrials.gov Identifier:
    NCT04681248
    Other Study ID Numbers:
    • DEK-DKK1-P206
    First Posted:
    Dec 23, 2020
    Last Update Posted:
    Apr 6, 2022
    Last Verified:
    Apr 1, 2022

    Study Results

    No Results Posted as of Apr 6, 2022