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Clinical trial intelligence for biotech diligence. Search source-linked clinical trial records, open structured report previews and unlock premium diligence workflows.

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TrialSignal provides research intelligence only. Reports and IP notes are not medical, legal, regulatory, investment, patentability or freedom-to-operate advice.

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Diligence-ready clinical trial intelligence

Turn clinical trial searches into diligence-ready intelligence.

Search public trial registries, index missing studies, compare sponsors and assets, and unlock source-linked reports with AI-assisted analysis and IP context.

Search public trial dataView a sample intelligence report

Registry-first

source provenance

AI-assisted

normalization

PDF-ready

analyst reports

NCT
IP
AI

Indexed report

GLP-1 obesity trial landscape

Source record verified

Sponsor and phase extracted

Patent landscape queued

Analyst workspace

Trials
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01

Search registries

02

Index reports

03

Export diligence
Public indexed search

Product scope

One workflow for search, reports, folders and IP follow-up.

Visitors can test public search before registration. Registered users can unlock individual reports, buy credits or subscribe for folders, exports, AI Q&A and patent enrichment requests.

Search that creates report cards

When a study is not already indexed, the search flow can ingest it and turn it into an internal TrialSignal report preview.

Diligence-grade structure

Each report separates sponsor, indication, intervention, outcomes, eligibility, contacts, source freshness, IP status and AI analysis.

Built for lean teams

Pay per report, buy project credits or subscribe monthly without committing to enterprise-priced intelligence platforms.

Recently indexed trial reports

Fresh report previews from the live index.

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NCT07294612Not ApplicableJul 02, 2026

Use of Platelet-Rich Fibrin in Bladder Exstrophy Repair: A Prospective Study

Bladder Exstrophy-Epispadias Complex · Target: Platelet-rich fibrin (PRF) as a biological adjunct in surgical repair, enhancing wound healing through growth factors and cytokines derived from autologous blood.

Open
NCT05944731Not yet recruitingJul 02, 2026

Use of Continuous Glucose Monitoring Devices Among People Living With Type 1 Diabetes in Kenya: A Three-arm Pragmatic Randomized Study on the Effectiveness, Feasibility, Acceptability, and Cost.

Type 1 Diabetes · Target: Continuous Glucose Monitoring Devices (CGMs) for diabetes management

Open
NCT03066154Phase 1Jul 02, 2026

Weekly ModraDoc/r in Combination With Hormonal Treatment and High-dose Intensity-modulated Radiation Therapy in Patients With High-risk Early Stage Prostate Cancer

Prostatic Neoplasms · Target: Docetaxel acts as a microtubule inhibitor, enhancing radiosensitivity in prostate cancer cells.

Open
NCT05142241Phase 2Jul 02, 2026

Rapid Analysis and Response Evaluation of Combination Anti-Neoplastic Agents in Rare Tumors (RARE CANCER) Trial: RARE 2 Talazoparib and Temozolomide

Adrenal Gland Pheochromocytoma · Target: Poly (ADP-ribose) polymerase (PARP) inhibition and DNA damage via alkylating agent mechanism.

Open
NCT00111683Phase 1/2Jul 02, 2026

A Phase I/II Dose Escalation Study of MK0457 in Patients With Leukemia

Chronic Myelogenous Leukemia in Blast Crisis · Target: Aurora kinase and BCR-ABL

Open
NCT04189783Phase 2Jul 02, 2026

Randomized Controlled Trial of Repeat vs. Single Quadratus Lumborum Block to Reduce Opioid Prescriptions After Open Resection of Retroperitoneal Sarcoma ("RESQU-SARC" Trial)

Retroperitoneal Sarcoma · Target: Liposomal bupivacaine injection (Quadratus Lumborum Block)

Open
NCT02654769Phase 3Jul 02, 2026

Multicenter Randomized Double-Blind Vehicle-Controlled Parallel Group Study to Determine the Therapeutic Equivalence of Generic Ingenol Mebutate Gel 0.05% and Picato® Gel 0.05% in Subjects With Actinic Keratosis on the Trunk or Extremities

Actinic Keratosis · Target: Ingenol Mebutate (mechanism of action involves inducing cell death in keratinocytes and promoting local immune response)

Open
NCT04751773Not applicable (interventional study without drug/device classification)Jul 02, 2026

Postoperative Exercise Training in Patients With Colorectal Liver Metastases Undergoing Surgery (ELMA)

Colorectal Liver Metastasis · Target: Not specified; focuses on the modulation of surgical stress response through exercise training in colorectal liver metastases patients.

Open
NCT02740270Phase 1/IbJul 02, 2026

A Phase I/Ib Open-label, Multi-center, Dose Escalation Study of GWN323 (Anti-GITR) as a Single Agent and in Combination With PDR001 (Anti-PD-1) in Patients With Advanced Solid Tumors and Lymphomas

Solid Tumors · Target: GITR (Glucocorticoid-Induced TNFR-Related Protein) and PD-1 (Programmed Cell Death Protein 1)

Open
NCT01964170Phase 3Jul 02, 2026

ASP3550 Phase III Study - An Open-Label, Active-Controlled, Parallel-Arm Study, Comparing ASP3550 With Goserelin Acetate in Patients With Prostate Cancer -

Prostate Cancer · Target: Gonadotropin-releasing hormone (GnRH) receptor

Open

Browse intelligence directories

Explore validated clusters by modality, then move into full indication and target directories from the intelligence hub.

behavioral interventioncell therapycombination therapygene therapymedical devicemicrobiome therapymonoclonal antibodyprotein therapy
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How it works

Move from public registry search to a source-linked diligence workflow.

Source-linked trial data

Search structured public trial records with NCT identifiers, sponsor fields and direct ClinicalTrials.gov source links.

AI-assisted normalization

Normalize targets, therapeutic modalities and indications while preserving raw registry values for auditability.

Analyst-ready reports

Open source-linked previews and upgrade when you need folders, exports, IP analysis and report Q&A.

Report anatomy

See what a paid report is built to answer.

Every report separates registry facts, normalized fields, AI analysis and IP research status so users can see what is sourced, what is inferred and what still needs professional validation.

Open sample report

Source & freshness

NCT ID, ClinicalTrials.gov link, source update date, internal sync and provenance badges.

Protocol intelligence

Study design, outcomes, eligibility, interventions, contacts and registry-derived fields.

Patent/IP layer

Verified patent rows when available, broader asset landscape and enrichment request status.

Analyst export

Branded PDF-ready structure for meetings, diligence notes and folder-level synthesis.

What premium unlocks

Reports that feel like an analyst deliverable, not a registry dump.

Reduce manual registry review into a repeatable report workflow.
Separate source records from AI-normalized and AI-generated content.
Turn searches into indexed internal report cards instead of external links.
Package trial sets into meeting-ready pipeline reports.
View sample report

Single-trial diligence brief

A structured asset view with sponsor, indication, intervention, outcomes, eligibility, contacts, source freshness and premium AI context.

Patent/IP work-up

Verified patent rows when available, plus clearly separated patentability and freedom-to-operate research notes for analyst follow-up.

Board-ready PDF export

A branded report export designed for meetings, with provenance, taxonomy, executive summary, source sections and research disclaimers.

Folder synthesis

Save multiple trials into a pipeline and generate a multi-report brief comparing readouts, sponsors, risks and next diligence checks.

Simple pricing

Choose the access model that fits the diligence job.

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Founders offer

5-day premium trial with code FOUNDERS5

Try unlimited reports, folders, AI assistant and exports before the €149/month subscription starts.

Single report

€29 one-time

Unlock one full source-linked report when you need a fast answer.

Credit bundles

€99, €249 or €599

Buy 5, 15 or 50 report credits for project-based research without recurring billing.

Monthly access

€149/month

Unlimited reports, folders, AI assistant, exports and multi-report synthesis.

Public sample

View a verified intelligence preview before creating an account.

This example links back to the original registry source and includes the latest available source or internal indexing timestamp.

NCT07294612Jul 02, 2026

Use of Platelet-Rich Fibrin in Bladder Exstrophy Repair: A Prospective Study

The study conducted by the National Children's Medical Center in Uzbekistan evaluates the use of autologous platelet-rich fibrin (PRF) in bladder exstrophy repair, a rare pediatric condition. With a small patient population of 20, the trial aims to demonstrate a reduction in postoperative complications, particularly penopubic fistula formation. If successful, this could position PRF as a valuable adjunct in pediatric urology, potentially expanding its application in other surgical contexts. The market for advanced wound healing products is growing, driven by increasing surgical procedures and a focus on reducing complications. However, the limited scope of this trial may restrict immediate commercial viability without further studies to validate findings across larger populations. Competitive analysis should consider existing biological and synthetic alternatives in wound healing.

Source: ClinicalTrials.gov

Timestamp: Jul 02, 2026

Sponsor: National Children's Medical Center, Uzbekistan

Modality: protein therapy

Trust boundaries

Clear enough for analysts. Careful enough for regulated markets.

We summarize public and user-provided sources for research and commercial intelligence.
We do not provide medical advice, patient guidance, legal opinions or regulatory clearance.
AI-generated sections should be validated against primary sources before investment or clinical decisions.

Important notes

Research software, not professional advice.

TrialSignal provides software for professional research triage using public clinical trial records, automated normalization and clearly marked AI-assisted analysis. Platform outputs are informational and should be independently verified against primary sources.

Reports, patent notes, AI summaries and folder analyses are not medical advice, legal advice, regulatory advice, investment advice, patentability opinions or freedom-to-operate opinions. Users remain responsible for decisions and for obtaining qualified professional review where needed.

The current contracting and product operator is identified as TrialSignal. Replace this operational notice with counsel-reviewed legal entity, jurisdiction, refund and compliance language before broad commercial launch.