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Japanese

Jan. 20, 2015

May. 20, 2022

jRCT2080222723

Phase IIa Study of F-1311 in Patients with Prostate Cancer

Phase IIa Study of F-1311 in Patients with Prostate Cancer

May. 27, 2016

No

-

version:
date:

PDRadiopharma Inc.

-

-

s-clinicaltrial-info@pdradiopharma.com

PDRadiopharma Inc.

-

-

s-clinicaltrial-info@pdradiopharma.com

completed

Mar. 18, 2015

15

Interventional

multicenter, open-label

diagnostic purpose

2

-Biopsy confirmed presence of adenocarcinoma of the prostate gland.
-Gleason score >= 7
-PSA > 20 ng/mL

-Subjects have received or have been receiving treatment or medication for prostate cancer.
-Subjects have severe hepatic or renal dysfunction.

20age old over
No limit

Male

Prostate cancer

investigational material(s)
Generic name etc : F-1311
INN of investigational material : -
Therapeutic category code : 43- Radioactive medicines
Dosage and Administration for Investigational material : intravenous injection

control material(s)
Generic name etc : -
INN of investigational material : -
Therapeutic category code :
Dosage and Administration for Investigational material : -

efficacy
Ability of F-1311 to accumulate in prostate cancer

safety
Adverse events

PDRadiopharma Inc.
-
-
-
IRB of Yokohama City University Hospital
3-9, Fukuura, Kanazawaku, Yokohama, Kanagawa, Japan

-

-
approved

Feb. 17, 2015

JapicCTI-152775
Japan

History of Changes

No Publication date
10 May. 20, 2022 (this page) Changes
9 Dec. 17, 2018 Detail Changes
8 Oct. 22, 2018 Detail Changes
7 Oct. 22, 2018 Detail Changes
6 Nov. 24, 2015 Detail Changes
5 Nov. 24, 2015 Detail Changes
4 Mar. 04, 2015 Detail Changes
3 Mar. 04, 2015 Detail Changes
2 Jan. 20, 2015 Detail Changes
1 Jan. 20, 2015 Detail