Ignite Creation Date:
2024-05-06 @ 1:59 PM
Last Modification Date:
2024-10-26 @ 1:23 PM
Study NCT ID:
NCT04186156
Status:
WITHDRAWN
Last Update Posted:
2021-02-03
First Post:
2019-07-17
Brief Title:
A Study of Selective HDAC6 Inhibition With KA2507 in Advanced Biliary Tract Cancer
Sponsor:
Karus Therapeutics Limited
Organization:
Karus Therapeutics Limited
Study Overview
Official Title:
A Phase II Study of Selective HDAC6 Inhibition With KA2507 in Advanced Biliary Tract Cancer Previously Treated With Standard of Care Chemotherapy ABC-11
Status:
WITHDRAWN
Status Verified Date:
2021-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Study not progressing
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
To evaluate the preliminary efficacy of KA2507 an orally active potent and selective HDAC6 inhibitor in patients with advanced biliary tract cancer BTC previously treated with standard of care chemotherapy
Detailed Description:
To evaluate the efficacy of KA2507 an orally active potent and selective HDAC6 inhibitor in patients with advanced biliary tract cancer BTC previously treated with standard of care chemotherapy
ABC-11 is an open-label multi-centre study of HDAC6 inhibition using KA2507 in patients with advanced biliary tract cancer previously treated with standard of care chemotherapy
This is a single-arm single-stage phase II study designed using AHerns methodology
The primary objective of this study is to assess the preliminary efficacy of KA2507 in patients with advanced BTC previously treated with standard of care chemotherapy
A fixed daily dose of KA2507 800mg BID will be administered to all patients based on a phase I study KTP-003
ABC-11 is an open-label multi-centre study of HDAC6 inhibition using KA2507 in patients with advanced biliary tract cancer previously treated with standard of care chemotherapy
This is a single-arm single-stage phase II study designed using AHerns methodology
The primary objective of this study is to assess the preliminary efficacy of KA2507 in patients with advanced BTC previously treated with standard of care chemotherapy
A fixed daily dose of KA2507 800mg BID will be administered to all patients based on a phase I study KTP-003
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None