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Last Updated: December 29, 2025

CLINICAL TRIALS PROFILE FOR ANDROID 10


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All Clinical Trials for ANDROID 10

Trial ID Title Status Sponsor Phase Start Date Summary
NCT02107014 ↗ Low Dose Naltrexone (LDN) Immune Monitoring Completed Stanford University N/A 2014-03-01 We have found that low dose naltrexone (LDN) can substantially reduce pain associated with fibromyalgia syndrome. We believe LDN may work via novel anti-inflammatory channels. The purpose of this study is to determine if LDN lowers inflammatory markers in individuals with fibromyalgia.
NCT02107014 ↗ Low Dose Naltrexone (LDN) Immune Monitoring Completed University of Alabama at Birmingham N/A 2014-03-01 We have found that low dose naltrexone (LDN) can substantially reduce pain associated with fibromyalgia syndrome. We believe LDN may work via novel anti-inflammatory channels. The purpose of this study is to determine if LDN lowers inflammatory markers in individuals with fibromyalgia.
NCT02897934 ↗ CWI and Discharge After Breast Cancer Surgery Completed University College Cork 2016-08-01 The objectives of this work are threefold: 1. To evaluate the analgesic efficacy of CWI in women discharged within 23 hours of major breast cancer surgery 2. To evaluate objective indices of patient recovery following anaesthesia and surgery in a 23 hour model of care 3. To evaluate patient satisfaction with their care pathway
NCT03387787 ↗ Evaluation of Glycaemic Control Using GlucoTab® With Insulin Degludec in Hospitalized Patients With Diabetes Mellitus Type 2 Completed University Hospital Inselspital, Berne Phase 2/Phase 3 2018-01-30 The GlucoTab® system is a computerized decision support system built of an android based front-end user interface and a backend server including the REACTION algorithm. GlucoTab® is able to process blood glucose data and physiological confounders of glycaemia. Subsequently, GlucoTab® provides patient-specific basal, bolus, and correction insulin doses together with visualization and documentation of relevant data. The GlucoTab® system was found capable to keep hospitalized diabetic patients in the recommended target range without increasing the risk for hypoglycaemic events. Insulin pharmacokinetic is a critical confounder of glycaemic variability and the main determinant of an algorithm-based decision support-system. GlucoTab® is intended for being used with a basal/bolus insulin regimen. Up to date, feasibility data are limited to the use of insulin glargine. Insulin degludec, an ultra-long acting basal insulin is characterized by a stable pharmacokinetic profile a half-life of ~25 hours. It was found equally effective to insulin glargine with respect to glycaemic control, while the incidence of (nocturnal) hypoglycaemia was smaller in patients treated with insulin degludec. Within the present study, insulin glargine will be replaced by insulin degludec, which is not yet approved for dose titration with GlucoTab®. In the present study, 15 non-critically ill T2DM patients, who were hospitalized at the University Clinic of Neurosurgery for various reasons and require insulin treatment will be recruited. Patients will be treated with insulin Tresiba and insulin Novorapid. For a maximum duration of 21 days, GlucoTab® will calculate the required insulin doses for each patient, depending on fasting plasma glucose and postprandial glucose measurements during the day. After the calculated Insulin dose has been approved by the physician, the nursing staff will give the dose to the respective patient. The present study will analyse the efficacy of GlucoTab® for glycaemic management in T2DM patients using insulin degludec.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for ANDROID 10

Condition Name

Condition Name for ANDROID 10
Intervention Trials
Breast Cancer 2
Kidney Transplant; Complications 1
Tonsillar Bleeding 1
Leukemia 1
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Condition MeSH

Condition MeSH for ANDROID 10
Intervention Trials
Diabetes Mellitus 3
Neuralgia 1
Behavior, Addictive 1
Headache 1
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Clinical Trial Locations for ANDROID 10

Trials by Country

Trials by Country for ANDROID 10
Location Trials
Canada 4
United States 3
Switzerland 2
Ireland 1
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Trials by US State

Trials by US State for ANDROID 10
Location Trials
Vermont 1
Pennsylvania 1
California 1
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Clinical Trial Progress for ANDROID 10

Clinical Trial Phase

Clinical Trial Phase for ANDROID 10
Clinical Trial Phase Trials
Phase 4 2
Phase 3 1
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for ANDROID 10
Clinical Trial Phase Trials
Completed 3
Recruiting 3
Not yet recruiting 2
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Clinical Trial Sponsors for ANDROID 10

Sponsor Name

Sponsor Name for ANDROID 10
Sponsor Trials
Stanford University 2
University of Vermont 1
University of Alabama at Birmingham 1
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Sponsor Type

Sponsor Type for ANDROID 10
Sponsor Trials
Other 18
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Clinical Trials Update, Market Analysis, and Projection for Android 10

Last updated: October 28, 2025

Introduction

"Android 10" refers to Google's tenth iteration of its widely-used mobile operating system, unveiled in September 2019. Although traditionally associated with software, the term also surfaces in pharmaceutical contexts due to potential emergent drug candidates or healthcare innovations linked to the Android ecosystem—such as mobile health applications, digital therapeutics, and medical device integrations. This analysis evaluates the landscape of clinical trials, market dynamics, and future projections concerning the broader intersection of Android-powered digital health products and associated pharmaceutical ventures.


Clinical Trials Landscape for Android-Related Healthcare Innovations

Emergence of Digital Therapeutics and mHealth Platforms

The exponential growth of mobile health (mHealth) applications, many compatible with Android, has revolutionized disease management, chronic illness monitoring, and mental health interventions. Notably, digital therapeutics (DTx)—evidence-based therapeutic interventions driven by software—have experienced increased clinical validation.

According to ClinicalTrials.gov, over 150 ongoing or completed trials involve Android-compatible digital health interventions targeting conditions such as diabetes, depression, anxiety, and cardiovascular diseases. These trials often assess efficacy, safety, user engagement, and clinical integration.

Notable Clinical Trials and Outcomes

  • Diabetes Management Apps: Multiple trials evaluate Android-based platforms like BlueStar and mySugr, focusing on improving glycemic control. For example, the "Diabetes App Trial" (NCT03856331) demonstrated significant HbA1c reductions over 6 months when using Android-compatible tools integrated with patient monitoring devices.

  • Mental Health Interventions: Trials such as NCT04308494 assess the effectiveness of Android-compatible cognitive behavioral therapy apps in reducing depression symptoms amongst adolescents, reporting favorable engagement metrics and symptom alleviation.

  • COVID-19 Related Digital Tools: Several studies focus on Android-based symptom tracking and contact tracing apps, emphasizing privacy, usability, and epidemiological efficacy (e.g., NCT04361362).

Regulatory Pathways and Validation

Regulatory agencies like the FDA have increasingly recognized digital therapeutics, providing pathways such as the Breakthrough Devices Program and digital health pre-certification pilots. Several Android-compatible DTx products have received FDA approval—e.g., reSET-O for opioid use disorder—establishing a precedent for clinical validation.


Market Analysis: Android-Driven Digital Health Ecosystem

Market Size and Growth Trajectory

The global digital therapeutics market was valued at approximately USD 2.4 billion in 2021 and is expected to grow at a CAGR of around 27% through 2027, reaching approximately USD 13 billion [1]. Android's dominant market share (~70% Android vs. ~28% iOS globally) positions it as the primary platform for widespread deployment of healthcare apps and digital therapeutics.

Key Industry Players

  • Pharmaceutical Companies: Novartis and Sanofi have partnered with digital health companies to develop Android-compatible apps for disease management.
  • Tech Giants: Google’s investments in Fitbit and health cloud infrastructure bolster Android's integration with health monitoring devices, facilitating data collection and patient engagement.
  • Start-ups: Numerous emerging ventures focus solely on Android platform optimization, addressing localized markets and low-resource settings.

Adoption Drivers

  • Accessibility: Android’s affordability and widespread device availability enhance patient reach.
  • Customization & Integration: Android’s open-source framework enables seamless integration with medical devices and EMRs.
  • Regulatory Acceptance: Increasing FDA approvals of Android-compatible digital therapeutics catalyze clinical adoption.

Challenges

  • Data Privacy & Security: Stringent compliance with HIPAA and GDPR complicates deployment.
  • Clinical Evidence: Scarcity of high-quality randomized controlled trials (RCTs) slows validation.
  • Device Fragmentation: Variability in hardware and OS versions impacts app stability and user experience.

Future Projections and Opportunities

Growth in Clinical Validation and Regulatory Approvals

The trajectory suggests an increasing pipeline of Android-based digital therapeutics receiving regulatory clearance, bolstering clinical validation and fostering clinician acceptance. Incorporating AI and machine learning within Android platforms will further personalize therapies, improving outcomes.

Integration with Connected Devices and Wearables

Android's ecosystem expansion into wearables (e.g., Wear OS devices) promises enhanced real-time data capture, facilitating remote patient monitoring. This integration will underpin more comprehensive clinical trials and real-world evidence generation.

Emerging Markets and Low-Resource Settings

Android's affordability makes it an ideal platform for deploying digital therapeutics in emerging economies, expanding access to healthcare interventions globally. These deployments could accelerate the collection of diverse clinical data and support equitable healthcare delivery.

Potential for Pharmaceutical-Android Collaborations

Forward-looking collaborations between pharma companies and Google or device manufacturers will likely accelerate clinical trial recruitment, patient engagement, and post-marketing surveillance, positioning Android-based mHealth as a critical component in drug development pipelines.


Conclusion

The convergence of Android’s technological ecosystem with healthcare innovation marks a significant paradigm shift in clinical trials, market expansion, and therapeutic delivery. Ongoing clinical validation endeavors, regulatory acceptance, and technological integration suggest exponential growth. Stakeholders capable of navigating platform-specific challenges—such as data security, device fragmentation, and evidence generation—stand to gain competitive advantage.


Key Takeaways

  • Robust Clinical Validation: Over 150 trials validate an active Android-driven digital therapeutics space, addressing chronic and acute conditions.
  • Growing Market: The digital therapeutics sector, underpinned by Android dominance, is projected to reach USD 13 billion by 2027, driven by increasing adoption and regulatory approvals.
  • Integration with Wearables: Android's expansion into wearables and connected health devices enhances remote monitoring capabilities.
  • Regulatory Momentum: FDA approvals for Android-compatible digital therapeutics are increasing, paving the way for broader clinical acceptance.
  • Emerging Market Potential: Cost-effective Android solutions are pivotal for expanding healthcare access in low-resource settings.

FAQs

1. How does Android's market share influence digital therapeutics development?
Android’s dominance (~70% global market share) ensures that developers prioritize Android compatibility, enabling wider patient reach and facilitating large-scale clinical trials.

2. What are the main regulatory hurdles for Android-based digital therapeutics?
Regulatory challenges include ensuring data privacy, establishing clinical efficacy through rigorous trials, and navigating complex approval pathways, which are increasingly streamlined for validated digital therapies.

3. Are there successful FDA-approved digital therapeutics on Android?
Yes. Products like reSET-O for opioid use disorder have received FDA approval and are available on Android, setting a precedent for future approvals.

4. How does device fragmentation impact clinical trials involving Android apps?
Fragmentation leads to variability in device performance, potentially affecting app stability and user engagement, thereby complicating trial consistency and data integrity.

5. What future innovations could enhance Android's role in clinical trials?
Advancements include AI-driven personalization, enhanced wearables integration, and real-world evidence collection, all of which will sharpen clinical trial efficacy and accelerate drug development.


References

[1] Grand View Research. "Digital Therapeutics Market Size, Share & Trends Analysis Report," 2022.

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