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Precision for Medicine

Phase 2-3 SCLC Case Study: Strategic Site Selection Drove Recruitment

Phase 2-3 SCLC Case Study: Strategic Site Selection Drove Recruitment

Small Cell Lung Cancer (SCLC) accounts for roughly 10–11% of all lung cancer cases [1] globally, yet it remains one of the most aggressive and difficult-to-treat subtypes

With rapid progression and limited second-line options, SCLC trials face intense pressure to identify, screen, and enroll patients before disease advancement closes the therapeutic window. In this case study, we explore how a sponsor’s Phase 2–3 trial overcame feasibility challenges through targeted site selection and real-time recruitment analytics—ultimately achieving full enrollment across 26 countries.

Therapeutic Area 

Oncology 

Indication 

Small Cell Lung Cancer (SCLC) 

Study Phase 

2-3 

Patient Segment 

Adult, Second Line 

Patients 

480+ 

Sites 

195+ 

Countries 

26: Australia; Bulgaria; Canada; France; Georgia; Hong Kong, Hungary; India; Italy; Lithuania; Malaysia; Philippines; Poland; Russia; Serbia; Slovakia; South Korea; Spain; Taiwan, Thailand; Ukraine; United Kingdom; United States 

Design 

Open-label, randomized study comparing IP + comparator vs. comparator alone in relapsed/refractory SCLC 

 

The SCLC Recruitment Challenge 

This multinational trial faced three major hurdles: 

  • Compressed timelines: Patients needed to be screened and dosed within days of relapse
  • Global variability: Referral pathways and incidence rates varied widely across regions
  • High screen failure rates: Comorbidities and prior therapies often disqualified otherwise eligible patients

To address these, the sponsor partnered with Precision for Medicine to deploy a dynamic feasibility model and a flexible site activation strategy. 

Precision Feasibility in Action 

Initial projections were built using historical enrollment data, regional incidence, and site-level performance. As the trial progressed, real-time adjustments were made based on actual screening and randomization trends. 

Diagram 1, SmartArt diagram

A dual-line graph tracked projected feasibility versus adjusted actuals, enabling: 

  • Resource reallocation to high-performing regions 
  • Deprioritization of underperforming sites 
  • Sustained enrollment velocity despite early screen failures 

Spain Leads Global Recruitment 

Of the 480+ patients enrolled globally, Spain alone contributed 73 — over 15% of total enrolled. This success was driven by: 

  • Early site activation and streamlined contracting 
  • Strong investigator engagement
  • High patient identification rates

Other notable contributors included the United States (64 enrolled) and Russia, Korea, France and Georgia, each with smaller but consistent enrollment. 

Chart 1, Chart element

Top-Performing Sites 

The trial’s success hinged on a handful of standout sites. In Spain and the United States, investigators led the charge. The most successful sites shared key traits: 

  • Oncology specialization with SCLC experience
  • Efficient pre-screening workflows 
  • Strong patient trust and referral networks 

Lessons Learned 

  • Feasibility is dynamic: Static models can’t keep pace with real-world variability. Real-time data monitoring enabled agile decision-making. 
  • Site selection matters: A few high-performing sites can drive the majority of enrollment—if activated early and supported well. 
  • Global doesn’t mean slow: With the right strategy, multi-country trials can outperform single-region studies in both speed and diversity. 

In SCLC, Precision can mean the difference between delay and delivery 

This trial proved that even in rare, aggressive indications, global studies can succeed when feasibility is treated as a living model—not a static spreadsheet. With the right sites, the right data, and the right support, precision becomes more than a strategy—it becomes a standard. 

References

  1. Terrasse V. Global lung cancer incidence according to subtype: new study highlights rising adenocarcinoma rates linked to air pollution. International Agency for Research on Cancer. February 3, 2025.  https://www.iarc.who.int/wp-content/uploads/2025/02/pr361_E.pdf. Accessed December 1, 2025.