You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 24, 2025

CLINICAL TRIALS PROFILE FOR DECADERM


✉ Email this page to a colleague

« Back to Dashboard


All Clinical Trials for Decaderm

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00002798 ↗ Combination Chemotherapy With or Without Bone Marrow Transplantation in Treating Children With Acute Myelogenous Leukemia or Myelodysplastic Syndrome Completed National Cancer Institute (NCI) Phase 3 1996-08-01 Randomized phase III trial to compare the effectiveness of different chemotherapy regimens with or without bone marrow transplantation in treating children who have acute myelogenous leukemia or myelodysplastic syndrome. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining chemotherapy with bone marrow transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more cancer cells. It is not yet known which treatment regimen is more effective for acute myelogenous leukemia or myelodysplastic syndrome
NCT00016302 ↗ Combination Chemotherapy in Treating Patients With Newly Diagnosed Acute Lymphoblastic Leukemia Completed National Cancer Institute (NCI) N/A 2001-04-01 Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. This phase II trial is studying several different combination chemotherapy regimens to see how well they work in treating patients with newly diagnosed acute lymphoblastic leukemia
NCT00022737 ↗ Combination Chemotherapy With or Without Peripheral Stem Cell Transplant in Treating Children With Acute Lymphoblastic Leukemia Completed National Cancer Institute (NCI) Phase 3 2002-10-01 This phase II trial is studying how well combination chemotherapy with or without donor peripheral stem cell transplant works in treating children with acute lymphoblastic leukemia. Giving combination chemotherapy before a donor peripheral stem cell transplant helps stop the growth of cancer cells. It also helps stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Decaderm

Condition Name

Condition Name for Decaderm
Intervention Trials
Stage III Multiple Myeloma 11
Refractory Multiple Myeloma 11
Stage II Multiple Myeloma 11
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Condition MeSH

Condition MeSH for Decaderm
Intervention Trials
Multiple Myeloma 23
Neoplasms, Plasma Cell 22
Precursor Cell Lymphoblastic Leukemia-Lymphoma 10
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Locations for Decaderm

Trials by Country

Trials by Country for Decaderm
Location Trials
United States 140
Canada 10
Switzerland 1
China 1
Australia 1
This preview shows a limited data set
Subscribe for full access, or try a Trial

Trials by US State

Trials by US State for Decaderm
Location Trials
California 14
Minnesota 11
Washington 9
Arizona 7
Ohio 7
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Progress for Decaderm

Clinical Trial Phase

Clinical Trial Phase for Decaderm
Clinical Trial Phase Trials
Phase 3 5
Phase 2 21
Phase 1/Phase 2 7
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Status

Clinical Trial Status for Decaderm
Clinical Trial Phase Trials
Completed 22
Terminated 9
Active, not recruiting 4
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Sponsors for Decaderm

Sponsor Name

Sponsor Name for Decaderm
Sponsor Trials
National Cancer Institute (NCI) 33
Mayo Clinic 7
University of Washington 4
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Sponsor Type

Sponsor Type for Decaderm
Sponsor Trials
Other 39
NIH 33
Industry 4
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trials, Market Analysis, and Projections for Decaderm: A Comprehensive Overview

Introduction to Decaderm and Its Context

While the term "Decaderm" is not specifically mentioned in the provided sources, we can infer insights from similar contexts such as clinical trials, market trends, and drug delivery systems. This article will provide a general overview of how clinical trials, market analysis, and projections might be applied to a hypothetical drug like Decaderm, using relevant examples and data from similar fields.

The Importance of Clinical Trials

Clinical trials are the backbone of drug development, ensuring the safety and efficacy of new treatments. For a drug like Decaderm, clinical trials would be crucial in assessing its benefits and risks.

  • Trial Design and Participant Safety: Clinical trials involve rigorous design to maximize efficiency and maintain participant safety. A study on cabozantinib, for example, highlighted the importance of methodologically rigorous trials to assess patient benefit and burden over time[4].
  • Phases of Clinical Trials: Decaderm would likely go through multiple phases of clinical trials, starting from Phase I to Phase III, each phase evaluating different aspects such as safety, dosage, and efficacy.
  • Example: Ponsegromab Trials: The clinical trials for ponsegromab, a drug targeting cancer cachexia, showed promising results with significant weight gain and improved symptoms in participants. This demonstrates the potential impact of well-designed clinical trials on drug development[1].

Market Analysis for Decaderm

Market Size and Growth

The market for new drugs, especially those with innovative delivery systems, is growing rapidly.

  • Global Market Trends: The global clinical trials market is projected to grow from $61.58 billion in 2024 to $106.78 billion by 2032, at a CAGR of 7.1%. This growth is driven by the increasing prevalence of chronic diseases and the need for new treatments[3].
  • Transdermal Drug Delivery Systems: If Decaderm were to be delivered via a transdermal system, the market size and growth would be significant. The transdermal drug delivery systems market was valued at USD 66.20 billion in 2023 and is expected to grow at a CAGR of 11.9% from 2024 to 2030[2].

Regional Insights

The market for Decaderm would vary by region, influenced by factors such as healthcare infrastructure, research and development investments, and disease prevalence.

  • North America: This region is expected to be a major market due to its advanced healthcare infrastructure and significant investments in R&D. The U.S. accounted for the largest share of the transdermal drug delivery system market in North America in 2023[2].
  • Asia Pacific: This region is expected to grow the fastest due to increasing healthcare spending, evolving healthcare infrastructure, and high research and development intensity in countries like China and India[2][5].

Market Growth Drivers

Several factors would drive the market growth for Decaderm:

  • Growing Prevalence of Chronic Diseases: The increasing incidence of chronic diseases such as cardiovascular illnesses, diabetes, and arthritis would drive the demand for effective treatments like Decaderm[5].
  • Innovative Drug Delivery Systems: Transdermal delivery systems, for instance, offer regulated and sustained release of medicines, enhancing patient compliance and comfort. This would be a significant growth driver if Decaderm were to use such a system[5].
  • Government Funding and Reimbursement: Favorable reimbursement scenarios and government funding towards healthcare would also contribute to market growth[2].

Safety and Efficacy

Ensuring the safety and efficacy of Decaderm would be paramount.

  • Side Effects and Safety Profile: The safety profile of Decaderm would be closely monitored during clinical trials. For example, ponsegromab showed few side effects and was considered safer than traditional appetite stimulants[1].
  • Clinical Benefits: The drug would need to demonstrate significant clinical benefits, such as improved symptoms and quality of life for patients. Ponsegromab’s ability to help patients gain weight and improve their physical activity is a strong example of such benefits[1].

Future Projections

Clinical Trials Expansion

If initial clinical trials for Decaderm show promising results, larger trials would be necessary to confirm these findings.

  • Example: Ponsegromab Trials: Pfizer is planning to launch a larger trial of ponsegromab next year based on the positive results from the initial trial. This could lead to the drug’s approval by regulatory bodies[1].

Market Expansion

The market for Decaderm could expand significantly if it gains approval and demonstrates long-term safety and efficacy.

  • Transdermal Drug Delivery Systems Market: The market for transdermal drug delivery systems is expected to grow substantially, driven by the need for innovative and effective treatment methods. Decaderm, if delivered transdermally, could benefit from this growth[2][5].

Key Takeaways

  • Clinical Trials: Rigorous clinical trials are essential for assessing the safety and efficacy of Decaderm.
  • Market Growth: The market for Decaderm would be driven by the growing prevalence of chronic diseases, innovative drug delivery systems, and favorable government policies.
  • Safety and Efficacy: Ensuring the safety and efficacy of Decaderm through thorough clinical trials is crucial for its success.
  • Regional Insights: The market for Decaderm would vary by region, with North America and the Asia Pacific expected to be significant markets.

FAQs

Q: What is the significance of clinical trials in drug development?

A: Clinical trials are crucial for ensuring the safety and efficacy of new drugs. They help in assessing the benefits and risks of the drug and are essential for regulatory approval.

Q: How does the market for transdermal drug delivery systems impact Decaderm?

A: If Decaderm is delivered via a transdermal system, it would benefit from the growing market for transdermal drug delivery systems, which is driven by the need for innovative and effective treatment methods.

Q: What factors drive the market growth for new drugs like Decaderm?

A: The market growth for Decaderm would be driven by the growing prevalence of chronic diseases, innovative drug delivery systems, and favorable government policies and reimbursement scenarios.

Q: How important is the safety profile of a new drug like Decaderm?

A: The safety profile of Decaderm is critical. A drug with few side effects and a strong safety profile, like ponsegromab, is more likely to gain regulatory approval and market acceptance.

Q: What role do regional markets play in the success of Decaderm?

A: Regional markets, particularly North America and the Asia Pacific, would play a significant role in the success of Decaderm due to their advanced healthcare infrastructure, high research and development investments, and growing healthcare spending.

Sources

  1. National Cancer Institute: "Ponsegromab Potentially Effective Against Cachexia" - October 17, 2024.
  2. Grand View Research: "Transdermal Drug Delivery System Market Size Report, 2030".
  3. Fortune Business Insights: "Clinical Trials Market SIZE, SHARE | GROWTH REPORT [2032]".
  4. PubMed: "Assessing patient burden and benefit: A decade of cabozantinib ..." - April 15, 2024.
  5. GlobeNewswire: "Transdermal Drug Delivery Systems Market Size/Share Envisaged To Grow USD 40.01 Billion By 2032 at 4.3% CAGR - Polaris Market Research" - March 11, 2024.

More… ↓

⤷  Try for Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.