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Last Updated: March 24, 2025

CLINICAL TRIALS PROFILE FOR HYDROCORTISONE SODIUM SUCCINATE


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All Clinical Trials for Hydrocortisone Sodium Succinate

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00002757 ↗ TITLE:Less Intensive Therapy for Children With Non-Hodgkin's Lymphoma Completed Children's Cancer and Leukaemia Group Phase 3 2001-06-01 RATIONALE: Less intensive therapy may attain in the same results as intensive therapy in children with non-Hodgkin's lymphoma. PURPOSE: Randomized phase III trial to study the effectiveness of less intensive therapy for children who have non-Hodgkin's lymphoma.
NCT00002757 ↗ TITLE:Less Intensive Therapy for Children With Non-Hodgkin's Lymphoma Completed National Cancer Institute (NCI) Phase 3 2001-06-01 RATIONALE: Less intensive therapy may attain in the same results as intensive therapy in children with non-Hodgkin's lymphoma. PURPOSE: Randomized phase III trial to study the effectiveness of less intensive therapy for children who have non-Hodgkin's lymphoma.
NCT00002757 ↗ TITLE:Less Intensive Therapy for Children With Non-Hodgkin's Lymphoma Completed Societe Francaise Oncologie Pediatrique Phase 3 2001-06-01 RATIONALE: Less intensive therapy may attain in the same results as intensive therapy in children with non-Hodgkin's lymphoma. PURPOSE: Randomized phase III trial to study the effectiveness of less intensive therapy for children who have non-Hodgkin's lymphoma.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Hydrocortisone Sodium Succinate

Condition Name

Condition Name for Hydrocortisone Sodium Succinate
Intervention Trials
Leukemia 5
Untreated Childhood Acute Lymphoblastic Leukemia 4
Sepsis 3
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Condition MeSH

Condition MeSH for Hydrocortisone Sodium Succinate
Intervention Trials
Leukemia 17
Leukemia, Lymphoid 16
Precursor Cell Lymphoblastic Leukemia-Lymphoma 16
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Clinical Trial Locations for Hydrocortisone Sodium Succinate

Trials by Country

Trials by Country for Hydrocortisone Sodium Succinate
Location Trials
United States 313
Canada 41
Australia 22
New Zealand 6
Puerto Rico 4
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Trials by US State

Trials by US State for Hydrocortisone Sodium Succinate
Location Trials
California 11
Massachusetts 10
Ohio 10
New York 10
Utah 9
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Clinical Trial Progress for Hydrocortisone Sodium Succinate

Clinical Trial Phase

Clinical Trial Phase for Hydrocortisone Sodium Succinate
Clinical Trial Phase Trials
Phase 3 9
Phase 2/Phase 3 1
Phase 2 10
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Clinical Trial Status

Clinical Trial Status for Hydrocortisone Sodium Succinate
Clinical Trial Phase Trials
Completed 11
Active, not recruiting 5
Not yet recruiting 4
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Clinical Trial Sponsors for Hydrocortisone Sodium Succinate

Sponsor Name

Sponsor Name for Hydrocortisone Sodium Succinate
Sponsor Trials
National Cancer Institute (NCI) 11
Children's Oncology Group 6
Boston Children's Hospital 2
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Sponsor Type

Sponsor Type for Hydrocortisone Sodium Succinate
Sponsor Trials
Other 40
NIH 11
Industry 6
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Hydrocortisone Sodium Succinate: Clinical Trials, Market Analysis, and Projections

Introduction to Hydrocortisone Sodium Succinate

Hydrocortisone sodium succinate is a widely used corticosteroid that targets the glucocorticoid receptor, influencing various physiological processes including immune response regulation, metabolism, and stress response. Here, we will delve into the current clinical trials, market analysis, and future projections for this drug.

Clinical Trials Update

SHIPSS Trial: Hydrocortisone in Pediatric Septic Shock

One significant clinical trial involving hydrocortisone is the SHIPSS (Stress Hydrocortisone In Pediatric Septic Shock) trial. This multi-institutional, prospective, randomized, double-blinded, placebo-controlled trial aims to evaluate the benefits and risks of adjunctive hydrocortisone in children with fluid and vasoactive-inotropic refractory septic shock. The trial hypothesizes that hydrocortisone will reduce the incidence of new and progressive organ dysfunction and improve health-related quality of life (HRQL) outcomes at 28 and 90 days post-enrollment[1].

Hydrocortisone in Severe Community-Acquired Pneumonia

A recent phase 3 trial published in 2023 investigated the use of hydrocortisone in adults with severe community-acquired pneumonia. The study found that patients receiving hydrocortisone had a lower risk of death by day 28 compared to those receiving a placebo. Additionally, the hydrocortisone group had lower rates of mechanical ventilation and vasopressor therapy initiation. This trial highlights the potential benefits of hydrocortisone in reducing mortality and improving outcomes in severe infections[3].

Market Analysis

Current Market Size and Segmentation

The hydrocortisone sodium succinate market was valued at USD 150 million in 2023 and is segmented based on type (injectable, oral tablets, creams), application (inflammatory conditions, allergic reactions, autoimmune diseases, endocrine disorders), and geographical regions (North America, Europe, Asia-Pacific, South America, and Middle-East and Africa)[2].

Growth Drivers

The market is driven by several factors, including the rising incidence of autoimmune and inflammatory diseases such as asthma and arthritis, which require efficient corticosteroid therapy. The benefits of corticosteroids in treating both acute and chronic illnesses are becoming more widely recognized, contributing to market expansion. Advances in drug formulation and delivery techniques, higher healthcare costs, and improved access to medical care in emerging nations also fuel market growth[2][4].

Market Projections

The hydrocortisone sodium succinate market is expected to grow at a Compound Annual Growth Rate (CAGR) of 6% from 2024 to 2031, reaching a projected value of USD 233.81 million by 2031. This growth is supported by increasing demand for corticosteroid therapy, continuous research and development to improve medication efficacy, and supportive government policies and healthcare infrastructure expansion[2][4].

Therapeutic Areas and Indications

Hydrocortisone sodium succinate has a broad range of therapeutic applications, including:

  • Adrenal Insufficiency: Used to treat conditions where the adrenal glands do not produce enough cortisol.
  • Infectious Diseases: Such as severe community-acquired pneumonia, where it has shown to reduce mortality.
  • Immune System Diseases: Including autoimmune diseases and allergic reactions.
  • Endocrinology and Metabolic Diseases: For conditions like thyrotoxicosis.
  • Eye Diseases: Various ocular conditions.
  • Hematologic Diseases: Blood-related disorders.
  • Respiratory Diseases: Asthma and other respiratory conditions.
  • Skin and Musculoskeletal Diseases: Skin conditions and musculoskeletal disorders[5].

R&D Innovations and Drug Patents

Hydrocortisone sodium succinate, developed by Pfizer Japan, Inc., has been approved in multiple countries since its first approval in the United States in April 1955. The drug has successfully completed clinical trials and demonstrated safety and efficacy. Ongoing R&D focuses on improving drug formulations and delivery methods to enhance therapeutic effects and reduce adverse events[5].

Key Takeaways

  • Clinical Trials: Ongoing trials like SHIPSS and recent studies on severe community-acquired pneumonia highlight the potential benefits of hydrocortisone in critical care settings.
  • Market Growth: The market is expected to grow significantly, driven by increasing demand for corticosteroid therapy and advancements in drug formulations.
  • Therapeutic Applications: Hydrocortisone sodium succinate is used in a wide range of therapeutic areas, including adrenal insufficiency, infectious diseases, and autoimmune diseases.
  • R&D Innovations: Continuous research aims to improve the efficacy and safety of hydrocortisone sodium succinate.

FAQs

What is the primary hypothesis of the SHIPSS trial?

The primary hypothesis of the SHIPSS trial is that hydrocortisone will decrease the incidence of new or progressive organ dysfunction and the proportion of subjects with poor outcomes, defined as death or severely impaired health-related quality of life (HRQL), in children with septic shock[1].

How does hydrocortisone sodium succinate impact mortality in severe community-acquired pneumonia?

Hydrocortisone sodium succinate has been shown to reduce the risk of death by day 28 in patients with severe community-acquired pneumonia compared to those receiving a placebo[3].

What are the key drivers of the hydrocortisone sodium succinate market growth?

The market growth is driven by the rising incidence of autoimmune and inflammatory diseases, advances in drug formulations, higher healthcare costs, and improved access to medical care in emerging nations[2][4].

In which therapeutic areas is hydrocortisone sodium succinate commonly used?

Hydrocortisone sodium succinate is used in various therapeutic areas including adrenal insufficiency, infectious diseases, immune system diseases, endocrinology and metabolic diseases, eye diseases, hematologic diseases, respiratory diseases, and skin and musculoskeletal diseases[5].

What is the projected market value of hydrocortisone sodium succinate by 2031?

The hydrocortisone sodium succinate market is expected to reach USD 233.81 million by 2031, growing at a CAGR of 6% from 2024 to 2031[2].

Sources

  1. UCSF Clinical Trials: Stress Hydrocortisone In Pediatric Septic Shock - UCSF Clinical Trials.
  2. Market Research Intellect: Hydrocortisone Sodium Succinate Market Size and Projections.
  3. PubMed: Hydrocortisone in Severe Community-Acquired Pneumonia.
  4. Market Research Pulse: Hydrocortisone Sodium Succinate Market Trends, Scope And Outlook.
  5. Patsnap Synapse: Hydrocortisone Sodium Succinate's R&D Progress.

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