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hydrocortisone

Generic: HYDROCORTISONE ACETATE·Brand: ACTICORT, AEROSEB-HC, ALA-CORT, ALA-SCALP, ALKINDI SPRINKLE, ANUSOL HC, Ala-Cort, Ala-Quin, Ala-Scalp, Alcortin, Alcortin A, Alkindi, Alocane Anti-Itch, Ana-Lex, Analpram HC, Anucort-HC, Anusol HC, Aquanil HC, Aquaphor Itch Relief, BALNEOL-HC, BETA-HC, Beta-HC, CARMOL HC, CETACORT, COLOCORT, CORT-DOME, CORTEF, CORTEF ACETATE, CORTENEMA, CORTIFOAM, CORTRIL, Caldecort, Cipro HC, Cortaid, Cortane-B, Cortef, Cortenema, Corticool, Cortifoam, Cortisporin, Cortisporin-TC, Cortizone, DERMACORT, DRICORT, Dermacort, Dermazene, Dermtex HC, ELDECORT, EPICORT, Epifoam, FLEXICORT, GLYCORT, Gynecort, H-CORT, HC #1, HC #4, HC (HYDROCORTISONE), HEMSOL-HC, HI-COR, HYDRO-RX, HYDROCORTISONE, HYDROCORTISONE ACETATE, HYDROCORTISONE IN ABSORBASE, HYDROCORTISONE VALERATE, HYDROCORTONE, HYTONE, Hemmorex, Hemorrodil Plus, Hemril, Instacort, KHINDIVI, Kera-HC, Khindivi, Locoid, MICORT-HC, Malacetic, MiCort-HC, Monistat Itch Relief, NOGENIC HC, NUTRACORT, Neo-Polycin HC, Novacort, Nucort, Nuzon, ORABASE HCA, Oticin HC, PENECORT, PROCTOCORT, Pandel, Pramosone, Procort 1.85/1.15, Procto-Kit, Procto-Med, Procto-Pak, Proctocort, Proctofoam-HC, Proctosol, Proctozone HC, Recort Plus, STIE-CORT, SYNACORT, Sarnol-HC, Scalacort, Scalpicin Itch Relief, Solu-Cortef, TEXACORT, Texacort, U-CORT, U-Cort, Vagisil Satin, Vanoxide-HC, Vytone, WESTCORT, Westcort, Xerese, Z-Pram, ZyPram

hydrocortisone: 17 clinical trials tracked.

hydrocortisone evidence translation

What we can confirm

17 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about hydrocortisone, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence6 indications · 8 study sponsors
Clinical Trials (17)showing 10 most recent

Intermediate-size Expanded Access of Remestemcel-L, Human Mesenchymal Stromal Cells, for Multisystem Inflammatory Syndrome in Children (MIS-C) Associated With Coronavirus Disease (COVID-19)

No longer available
Expanded AccessMesoblast International Sàrl

A Phase 2 Trial of Early Enhanced Interventions to Prevent ICANS After CD19 CAR T Therapy in Patients With Non-Hodgkin Lymphoma: Lazarus Trial

NCT07763210·Phase 2
Not yet recruiting

Primary endpoint: Efficacy of IT therapy to reduce high-grade ICANS in participants who receive axi-cel in NHL compared to historical experience

InterventionalRandomizedopen59 targetStarted 2026-10Completion 2030-101 site · United StatesVanderbilt-Ingram Cancer Center

Open-label, Phase I/II Study to Evaluate Safety and Efficacy of Asciminib With Chemotherapy Followed by Asciminib Plus Blinatumomab in Pediatric, Adolescent, and Young Adults With Relapsed or Refractory BCR::ABL1-positive (Philadelphia Positive, Ph+) or BCR::ABL1-like (Ph-like) ALL

NCT07387926·Phase 1/Phase 2·NVS
Recruiting

Primary endpoint: Part 1 Dose Escalation: Incidence of Dose Limiting Toxicities (DLTs) occurring during cycle 1 (debulking induction)

Interventionalopen50 targetStarted 2026-07Completion 2036-051 site · IsraelNovartis Pharmaceuticals

A Pilot Study of Intrathecal Topotecan and Maintenance Chemotherapy in the Post-consolidation Setting for the Treatment of High-risk Embryonal Central Nervous System Tumours in Children Less Than 6 Years of Age

NCT06942039·Early Phase 1·AIM
Recruiting

Primary endpoint: To determine the feasibility of adding intrathecal (IT) topotecan and maintenance therapy after high dose chemotherapy for treatment of newly diagnosed HR-EBTs in patients less than 6 years of age.

Interventionalopen15 targetStarted 2025-09Completion 2032-1212 sites · CanadaC17 Council

Safety and Efficacy of Topical Bacteriotherapy for Atopic Dermatitis Using Staphylococcus Hominis A9

NCT06504160·Phase 1
Recruiting

Primary endpoint: Time to the first Atopic Dermatitis (AD) flare.

InterventionalRandomizedquadruple86 targetStarted 2025-05Completion 2027-028 sites · United StatesNational Institute of Allergy and Infectious Diseases (NIAID)

A Phase 1 Clinical Study to Investigate the Safety and Pharmacokinetics of MK-5684 in China Participants With Metastatic Castration-Resistant Prostate Cancer

NCT06136598·Phase 1·MRK
Active, not recruiting

Primary endpoint: Number of Participants Who Experience an Adverse Event (AE)

Interventionalopen14 targetStarted 2024-01Completion 2026-033 sites · ChinaMerck Sharp & Dohme LLC

A Phase 3 Randomized, Open-label Study of MK-5684 Versus Alternative Abiraterone Acetate or Enzalutamide in Participants With Metastatic Castration-resistant Prostate Cancer (mCRPC) Previously Treated With Next-generation Hormonal Agent (NHA) and Taxane-based Chemotherapy (OMAHA-003)

NCT06136624·Phase 3
Recruiting

Primary endpoint: Overall Survival (OS) in Androgen Receptor Ligand Binding Domain (AR LBD) Mutation-Positive Participants

InterventionalRandomizedopen1,310 targetStarted 2023-12Completion 2030-0250 sites · Argentina, United StatesMerck Sharp & Dohme LLC

MK-5684-004: A Phase 3, Randomized, Open-label Study of Opevesostat Versus Alternative Abiraterone Acetate or Enzalutamide in Participants With Metastatic Castration-resistant Prostate Cancer (mCRPC) That Progressed On or After Prior Treatment With One Next-generation Hormonal Agent (NHA) (OMAHA-004)

NCT06136650·Phase 3
Recruiting

Primary endpoint: Radiographic Progression-Free Survival (rPFS)

InterventionalRandomizedopen1,314 targetStarted 2023-12Completion 2030-1250 sites · United StatesMerck Sharp & Dohme LLC

A Phase 1 Clinical Study to Investigate the Safety and Pharmacokinetics of MK-5684 in Japanese Participants With Metastatic Castration-resistant Prostate Cancer (mCRPC)

NCT06104449·Phase 1·MRK
Active, not recruiting

Primary endpoint: Number of Participants Who Experience a Dose-limiting Toxicity (DLT) as Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0 by the Investigator

Interventionalopen6 targetStarted 2023-11Completion 2026-043 sites · JapanMerck Sharp & Dohme LLC

A Phase I Study of Venetoclax in Combination With Cytotoxic Chemotherapy, Including Calaspargase Pegol, for Children, Adolescents and Young Adults With High-Risk Hematologic Malignancies

NCT05292664·Phase 1
Recruiting

Primary endpoint: Maximum tolerated dose (MTD)

Interventionalopen30 targetStarted 2023-03Completion 2030-075 sites · United StatesAndrew E. Place, MD