CASE STUDIES & RESULTS

Proven Results

Proven Results That Accelerate Clinical Research

Our technology platform has demonstrated 94% faster enrollment timelines, 75% reduced screen failures, and 85% patient retention across 200+ clinical trials.

94%
Faster Enrollment
75%
Reduced Failures
85%
Patient Retention
200+
Trials Supported

PLATFORM IMPACT

Platform Impact
10K+
Patients Enrolled
200+
Clinical Trials Supported
50+
Research Site Partners
94%
Faster Enrollment
(vs. traditional)
75%
Reduced Screen Failures
85%
Patient Retention
MIN
Avg Contact Time
(Not Days)

CASE STUDIES

Real results from real clinical trials

Case Study #1

ONCOLOGY TRIAL RESCUE

Phase II Breast Cancer Trial — Behind Timeline, At Risk of Cancellation

Oncology Trial
⚠ The Challenge
8 months behind enrollment timeline
Only 23 patients enrolled (target: 200)
$4.8M in delay penalties accumulating
Sites had exhausted patient databases
Sponsor considering trial cancellation
✓ Our Solution
Digital campaigns: Targeted Facebook, Instagram, and Google
Pre-screening: In-house team qualified every patient
Site coordination: Managed 12 sites in 6 states
Real-time analytics: Daily sponsor dashboard
★ The Results
147 patients in 4 months
Screen failure: 12% (vs. 48%)
$2.1M saved in penalties
Trial completed 3 months ahead

"Clinical Trial Solutions saved this trial. We went from considering cancellation to finishing early."

— Sponsor Project Director

Case Study #2

FDA DIVERSITY MANDATE COMPLIANCE

Phase III Cardiovascular Trial — Hispanic Enrollment Required for Regulatory Approval

!

The Challenge

• Required 40% Hispanic enrollment per FDA mandate
• Current enrollment only 12% Hispanic
• Sites lacked Hispanic patient access
• Regulatory approval at stake

Our Solution

Spanish-language campaigns: Full Spanish creative across TX, FL, CA, PR
Bilingual pre-screening: Native Spanish-speaking coordinators
Community partnerships: Hispanic health organizations
Demographic documentation: Detailed FDA tracking
Diversity
FDA Diversity
12% → 44%

★ The Results

12%→44%
Hispanic Enrollment
6 wks
Early Completion
100%
FDA Requirements Met
Zero
Regulatory Delays

"Clinical Trial Solutions not only met our diversity requirement—they exceeded it. Their bilingual capabilities are the real deal."

— CRO Diversity Lead

Case Study #3

RARE DISEASE RECRUITMENT

Phase I/II Genetic Disorder Trial — Ultra-Rare Population (<3,000 US Patients)

The Challenge

• Only ~3,000 diagnosed patients in entire US
• Needed 25 patients to meet enrollment
• Previous vendor failed to enroll a single patient in 6 months
• Complex eligibility with genetic confirmation required

Our Solution

Lookalike modeling: Custom audience based on condition-specific behaviors
Advocacy partnerships: Direct outreach through patient organizations
Nationwide reach: Telemedicine pre-screening removed geographic barriers
High-touch coordination: Dedicated coordinator for each patient

The Results

28 patients enrolled (exceeding 25-patient target)
40% lower cost-per-patient vs. industry benchmark
Enrollment completed in 5 months (vs. 18-month projection)
Zero dropout during treatment phase
CNS Neurology
Case Study #4
CNS/NEUROLOGY

MULTI-SITE COORDINATION

Phase III Alzheimer's Trial — Complex Screening, High Dropout Risk

The Challenge

Industry-leading 70%+ screen failure rate for AD trials. Caregiver involvement required—double the coordination. 20 sites nationwide with inconsistent performance. Previous 35% dropout rate threatening data integrity.

Our Solution

Caregiver-focused campaigns: Targeted adult children researching parent's condition. Extended pre-screening: 45-minute calls including cognitive pre-assessment. Dual coordination: Separate scheduling for patient and caregiver. Retention program: Weekly check-ins with both patient and caregiver.

38%
Screen Failure
(vs. industry 70%+)
12%
Dropout Rate
(vs. previous 35%)
100%
Timeline Met
(first time in portfolio)
9.2/10
Site Rating
(avg satisfaction)
Case Study #5

VACCINE TRIAL RAPID ENROLLMENT

Phase III Respiratory Vaccine — Urgent Timeline, High-Volume Requirement

Deadline
90 Days
Vaccine Trial
!

The Challenge

• 500 patients needed in 90 days
• Specific age and health criteria
• Seasonal urgency—window closing
• Multiple competing trials

Our Solution

High-volume campaigns: 2M+ impressions/week
Expanded call center: 500+ pre-screens/week
Site load balancing: Automated routing
Same-week scheduling: 72-hour booking

The Results

523 patients in 87 days
Seasonal window met
14% screen failure
22% under budget

THERAPEUTIC AREAS

Our platform has successfully recruited patients across all major therapeutic areas:

🎗️

Oncology

Breast, lung, prostate, melanoma, colorectal, leukemia, lymphoma, pancreatic, ovarian, brain tumors

❤️

Cardiovascular

Heart failure, hypertension, AFib, CAD, PAD, stroke prevention

🧠

Neurology/CNS

Alzheimer's, Parkinson's, MS, epilepsy, migraine, ALS, neuropathy

⚖️

Endocrinology

Type 1 & 2 diabetes, obesity, thyroid, NASH/NAFLD

🫁

Respiratory

Asthma, COPD, cystic fibrosis, pulmonary fibrosis

🧘

Mental Health

Depression, anxiety, PTSD, bipolar, schizophrenia, OCD, ADHD

Dermatology

Psoriasis, eczema, vitiligo, acne, HS

🩺

Gastrointestinal

Crohn's, ulcerative colitis, IBS, GERD, celiac

🧬

Rare Diseases

Genetic disorders, metabolic storage diseases, ultra-orphan conditions

💉

Vaccines

Respiratory, travel, HIV, hepatitis, infectious disease

Get Started

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