Statistical Design Software

The Modern Standard for Experimental Design

Stop paying $1,000+ for clunky desktop software. Run Group Sequential designs, CUPED, and Bayesian simulations directly in your browser.

51

Validation tests against PASS & nQuery

30%

Sample size reduction with CUPED

$99

Per month vs $4,995/yr for nQuery

Figure 1

O'Brien-Fleming Stopping Boundaries

gsDesign v3.6
432100.00.250.50.751.0Information FractionZ-valueEfficacy (α=0.025)Futility (β=0.10)

Parameters

DesignO'Brien-Fleming
Interim Analyses4
Alpha (one-sided)0.025
Power90%
Max Sample Size2,847
Expected N (H1)1,923

Output matches gsDesign R package v3.6.0

Why Zetyra

Clinical Rigor.
Regulatory Integrity.

Statistical engines built for the highest levels of scrutiny. Transparent, reproducible, and benchmarked against industry standards to support FDA- and EMA-ready trial design.

Standardized R-Backends

Eliminate “black box” calculations. Zetyra utilizes standardized R-backends for statistical legitimacy, providing full methodology transparency for your SAP.

High-Performance Simulation

Built for computational velocity. Run complex Monte Carlo simulations and adaptive design iterations at scale without legacy desktop latency.

Benchmarked Precision

Algorithms rigorously cross-validated against established standards, achieving numerical parity with industry-leading software.

Table 1

Validation Against Industry Standards

Industry StandardParity LevelGuideline Alignment
Two-sample t-test (Satterthwaite)Full ParityConsistent with ICH E9 principles
GSD (O'Brien-Fleming)Full ParityDesigned for FDA/EMA Stopping Rules
Bayesian Predictive PowerOptimizedSupports adaptive design frameworks

Adaptive Design Integrity

Optimize trial efficiency with precise Group Sequential boundaries. Use O'Brien-Fleming or Pocock spending functions to calculate stopping rules without compromising Type I error (α). Zetyra ensures that the preservation of the family-wise error rate is mathematically sound and fully reproducible.

Pricing

Simple Plans

Start free. Upgrade when you need advanced features. Cancel anytime.

Competitor pricing

nQuery Pro: $4,995/yr

Zetyra Pro: $99/mo

Free

The Essentials

$0/forever
  • Standard sample size calculator
  • Two-sample t-test
  • Interactive power curves
  • No signup required
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Pro

Recommended

Evidence Pro

$99/mo

$29/mo for .edu

  • CUPED variance reduction
  • Bayesian predictive power
  • Group sequential design (R-powered)
  • Survival power analysis
Start Free Trial

Team

Evidence Collective

$349/mo

5 seats included

  • Everything in Pro
  • Shared project library
  • Priority support
Start Team Trial

Enterprise

Custom

Contact
  • SSO / SAML
  • On-premise option
  • 21 CFR Part 11
Contact Sales

FAQ

Questions & Answers

Everything you need to know about Zetyra.

Have more questions?

Contact our team

We maintain an open-source validation suite with 51 automated tests against industry gold standards. Our GSD module matches the gsDesign R package within 0.005 z-score units. We also replicate published clinical trials (HPTN 083, HeartMate II) and validate CUPED/Bayesian calculations against analytical formulas. View our full validation suite at github.com/evidenceinthewild/zetyra-validation.

For Group Sequential designs, we use the industry-standard gsDesign R package directly in our backend. For CUPED and Bayesian simulations, we use custom Python implementations built on NumPy and SciPy, validated against published statistical methods and MCMC simulations.

Yes. Zetyra uses the same gsDesign R package that powers many FDA-approved clinical trial designs, and our calculations match industry-standard software. For regulatory submissions, we recommend including the exported PDF report (which lists all parameters and version numbers) alongside your Statistical Analysis Plan.

Yes. Pro users can export professional PDF reports that include all input parameters and results. We are also actively developing R script export for Group Sequential designs, allowing you to paste the exact generation code into your analysis plan.

We have a REST API available for Enterprise partners who need programmatic access to our calculators. Contact sales@zetyra.com if you need to integrate Zetyra into your internal workflow or run bulk calculations.

No. All plans are month-to-month. Cancel anytime with no questions asked.

Zetyra provides the same statistical accuracy (validated against both) at a fraction of the cost. PASS/nQuery offer broader legacy test coverage but require expensive desktop licenses ($1,295+/year). Zetyra focuses on modern clinical trial designs (GSD, CUPED), runs in your browser with no installation, and enables easy sharing—starting at $99/mo.

We treat your designs as confidential. All data is encrypted in transit (TLS 1.3) and at rest. Input parameters are processed in real-time and not stored unless you explicitly save a project. We never use your data to train models or share it with third parties.

Evidence Collective ($349/month) includes 5 team seats, everything in Pro, a shared project library, team commenting and review features, and priority email support. It's designed for biostatistics departments that need to collaborate on trial designs. Additional seats can be added for $49/month each.

Yes! Academic users with a .edu email get Evidence Pro for just $29/month—70% off the standard price. This applies to graduate students, postdocs, and faculty. Sign up with your .edu email to automatically receive the discount.

If you cancel your Pro subscription, you retain access until the end of your billing period. Afterwards, your account reverts to the free tier. Your saved projects remain in your account as read-only (you can view and export them, but not edit).