enzalutamide

Phase 1Completed

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Hype Score

Development Stage

✓

Pre-clinical

Phase 1

Phase 2

Phase 3

Approved

Indication / Disease

Severe Hepatic Impairment

Conditions

Severe Hepatic Impairment, Normal Hepatic Function

Trial Timeline

Aug 1, 2013 → Mar 1, 2014

NCT ID

NCT02138162

About enzalutamide

enzalutamide is a phase 1 stage product being developed by Astellas Pharma for Severe Hepatic Impairment. The current trial status is completed. This product is registered under clinical trial identifier NCT02138162. Target conditions include Severe Hepatic Impairment, Normal Hepatic Function.

Hype Score Breakdown

Clinical

Activity

Company

Novelty

Community

Clinical Trials (20)

NCT ID	Phase	Status	Start	Completion	Indication
NCT05404139	Phase 2	Recruiting	May 24, 2023	Mar 1, 2026	Metastatic Prostate Cancer
NCT02749903	Phase 2	Active	Sep 14, 2016	Jul 5, 2028	Salivary Cancer
NCT02799745	Phase 2	Completed	Jun 9, 2016	Aug 28, 2020	Prostate Cancer
NCT02750358	Phase 2	Active	May 19, 2016	May 1, 2026	Breast Cancer
NCT02605863	Phase 2	Terminated	Jan 1, 2016	Feb 1, 2018	Bladder Cancer
NCT02384382	Phase 2	Completed	Nov 30, 2015	May 3, 2019	Prostate Carcinoma Metastatic to the Bone
NCT02441517	Approved	Terminated	Oct 28, 2015	Mar 15, 2017	Metastatic Castration Resistant Prostate Cancer
NCT02507570	Phase 2	Completed	Sep 23, 2015	Jan 18, 2019	Prostate Carcinoma Metastatic to the Bone
NCT02495974	Pre-clinical	Completed	Sep 8, 2015	Feb 8, 2019	Metastatic Castration Resistant Prostate Cancer
NCT02203695	Phase 2	Completed	Mar 28, 2015	Dec 31, 2022	Adenocarcinoma of the Prostate
NCT02288936	Phase 2	Completed	Feb 5, 2015	Jul 22, 2019	Hormone-refractory Prostate Cancer
NCT02669771	Pre-clinical	Completed	Nov 30, 2014	Nov 30, 2018	Castration-resistant Prostate Cancer
NCT02124668	Phase 2	Completed	Sep 23, 2014	May 25, 2017	Castration-Resistant Prostate Cancer
NCT03297385	Phase 2	Completed	Aug 28, 2014	Apr 1, 2017	Prostate Cancer
NCT02116582	Approved	Completed	May 23, 2014	Sep 29, 2017	Metastatic Castration-Resistant Prostate Cancer
NCT02099864	Phase 2	Completed	Feb 5, 2014	Jul 8, 2024	Castration-Resistant Prostate Carcinoma
NCT01977651	Approved	Completed	Sep 25, 2013	Jan 11, 2019	Metastatic Castration-resistant Prostate Cancer (mCRPC)
NCT02138162	Phase 1	Completed	Aug 1, 2013	Mar 1, 2014	Severe Hepatic Impairment
NCT01889238	Phase 2	Completed	Jun 12, 2013	Jan 10, 2024	Advanced, Androgen Receptor Positive Triple Negative Breast Cancer
NCT01663415	Phase 2	Withdrawn	Aug 1, 2012	Oct 1, 2014	Metastatic Castration-Resistant Prostate Cancer

Competing Products

20 competing products in Severe Hepatic Impairment

See all competitors

Product	Company	Stage	Hype Score
Popliteal nerve block including liposomal bupivacaine + Adductor canal nerve block including liposomal bupivacaine + Continuous popliteal nerve block with normal saline + Popliteal nerve block with exclusively unencapsulated bupivacaine + Adductor canal nerve block with exclusively unencapsulated bupivacaine + Continuous popliteal nerve block with unencapsulated bupivacaine	Pacira Biosciences	Approved	80
Drotrecogin alfa (activated)	Eli Lilly	Phase 2	52
CT-P13 SC Auto-Injector + Placebo Auto-Injector	Celltrion	Phase 3	77
CT-P17 + EU-approved Humira	Celltrion	Phase 3	77
Afimkibart + Placebo	Chugai Pharmaceutical	Phase 3	77
Afimkibart + Placebo	Chugai Pharmaceutical	Phase 3	77
Afimkibart + Placebo	Chugai Pharmaceutical	Phase 3	77
CS-3150	Daiichi Sankyo	Phase 3	77
tacrolimus	Astellas Pharma	Approved	85
Isavuconazonium Injection [Cresemba] + Placebo	Astellas Pharma	Phase 3	77
Alefacept	Astellas Pharma	Approved	85
Placebo + SCD-044_Low Dose (Dose 1) + SCD-044_Intermediate Dose (Dose 2) + SCD-044_High Dose (Dose 3)	Sun Pharmaceutical	Phase 2	52
Tildrakizumab 100 mg + Placebo	Sun Pharmaceutical	Phase 3	77
Tildrakizumab + Placebo + Tildrakizumab + Tildrakizumab + Tildrakizumab + Etanercept + Placebo	Sun Pharmaceutical	Phase 2/3	65
Cefiderocol	Shionogi	Approved	85
eritoran tetrasodium + Placebo	Eisai	Phase 3	77
Donepezil HCl	Eisai	Approved	85
Donepezil Hydrochloride (Aricept)	Eisai	Approved	85
KHK4827 + Placebo	Kyowa Kirin	Phase 3	77
KHK4827 + Placebo	Kyowa Kirin	Phase 3	77

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