Educational research platform

Before you begin

Welcome to Peptide Relay

Explore source-linked research, practical tools, and Community Intelligence with evidence, interpretation, and personal experience kept clearly separated.

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Choose how you enter RelayYou can change your mind and create a workspace later.

No account is required for the Research Library, Learn, Compare, Stack Explorer, Community, or Tools. A free workspace is only required for private features such as My Relay, Protocol Tracker, saved work, following compounds, and managing Community Experiences.

Peptide Relay status

Public Alpha

v0.9.0

Building Relay with the community.

Relay is now feature-complete and has entered its first Public Alpha.

From this point forward, improvements are driven by real-world usage, community feedback, analytics, and research rather than internal feature planning.

Thank you for helping shape Relay.

What's NewWhat shipped in the current release
v0.9.0 — Public AlphaJuly 2026

Research Library

Thirty-five source-traceable compound and blend profiles with plain-English summaries, detailed science, evidence context, timelines, and references.

Learn

Peptide 101 and seven cornerstone guides for reading studies, mechanisms, evidence strength, personal experiences, and research uncertainty.

Compare

Side-by-side research context with shared, different, and unknown states—without inventing head-to-head conclusions.

Stack Explorer

Multi-compound pathway and evidence analysis with exact-combination limits and unanswered questions kept visible.

Community Experiences

Anonymous structured Experience Reports, separate story consent, verified follow-ups, moderation, and privacy-thresholded Community Intelligence.

Protocol Tracker

Private schedules, administrations, reflections, measurements, inventory, imports, lifecycle controls, and reconstitution support.

Reconstitution Hub

Single-compound and blend calculations, visual syringe and vial interpretation, reference marks, and private saved workspaces.

Relay-wide Search

One alias-aware search experience across public research and signed-in workspace destinations.

Mobile Optimization

Reliable touch selection, tighter information density, responsive tables and tabs, and mobile-first workflow refinement.

Motion System

One restrained motion language that explains state changes and respects reduced-motion preferences.

Platform Improvements

Database contract auditing, private-route indexing boundaries, public-route smoke tests, clearer recovery messages, and stronger protection against false-success writes.

RoadmapDirection without promised timelines

Roadmap items describe current direction. Public Alpha evidence may change their order or scope.

Now
  • Community growth
  • Bug fixes
  • UX improvements
  • Content expansion
Next
  • Relay+ features
  • Additional research tools
  • Expanded compound library
Future
  • Relay AI
  • Native iPhone app (planned)
  • Native Android app (planned)
Known IssuesMeaningful issues users may encounter
No known critical issues at this time.

Newly confirmed issues will appear here when they meaningfully affect the public experience.

FeedbackHelp improve the next release

Found a bug?Have a suggestion?

Submit feedback to help improve Relay
Version HistoryPublic releases and milestones
v0.9.0

Public Alpha

The first feature-complete public release candidate for Peptide Relay.

Released July 2026

Last updated July 2026 · Updated with every public release.

Simple first. Deeper when you want it.

Understand the differences that matter.

See the biggest similarities, differences, strengths, limitations, and unanswered questions first—then open the evidence behind them.

Compound comparison

Tesamorelin vs. Tirzepatide

Understand the meaningful overlap, differences, evidence, and unknowns—then go deeper only when you want to.

60-Second Summary

The answer first

Deeper evidence stays available below
Why compare them?

These records are compared to clarify how their mechanisms, research areas, and evidence maturity differ.

Current evidenceVery limited comparison

At least one comparison profile is still being completed. Use the underlying compound records for the evidence currently available.

✓ Shared

Shared Similarities

  • Both have controlled human research, although the questions and designs may differ.
  • Both have FDA-approved products for defined, product-specific indications.
⇄ Different

Biggest Difference

Tesamorelin is distinguished by tesamorelin stimulates the pituitary growth-hormone pathway. Controlled human evidence supports a narrow HIV-lipodystrophy indication; it is not approved as a general weight-loss drug; Tirzepatide is distinguished by dual agonist at GIP and GLP-1 receptors, with approved U.S. products and a much larger completed evidence base.

? Unknown

Biggest Unknown

No direct head-to-head study establishes how these compounds compare under the same population, dose, duration, and endpoints.

Key Takeaways

Tesamorelin is distinguished in the current record by tesamorelin stimulates the pituitary growth-hormone pathway. Controlled human evidence supports a narrow HIV-lipodystrophy indication; it is not approved as a general weight-loss drug. Tirzepatide is distinguished by dual agonist at GIP and GLP-1 receptors, with approved U.S. products and a much larger completed evidence base. Neither is objectively “better”; the useful question is which evidence record addresses the research question being asked.

Research matrix

Which question has stronger current support?

Evidence support, not a “better compound” score
Research questionStronger current supportExplanation
Human evidenceTirzepatide

Tesamorelin: Profile in progress. Tirzepatide: Mature human evidence.

Regulatory historyComparable

Tesamorelin: FDA approved for a defined indication. Tirzepatide: FDA approved for defined indications.

Mechanistic breadthTirzepatide

More named targets describes mechanistic breadth; it does not establish greater effectiveness.

Direct comparisonUnknown

Separate studies cannot establish comparative superiority.

Deeper when you want it

Explore the evidence and nuance

Every section is optional
Best-studied areas and pathway mapSee shared targets, unique pathways, and the research questions attached to each record.
Best-studied research areas

Tesamorelin

  • HIV-associated lipodystrophy
  • Visceral abdominal fat
  • Body composition
  • HIV-associated NAFLD / MASLD
Best-studied research areas

Tirzepatide

  • Obesity
  • Type 2 diabetes
  • Cardiometabolic outcomes

Pathway and research map

Shared foundation and unique questions

Shared pathways
  • No shared named receptor target in the current records.
Tesamorelin only
  • GHRHR
Tirzepatide only
  • GIPR
  • GLP-1R
Shared research areas
  • No exact shared research-area label in the current records.
Tesamorelin distinctions
  • HIV-associated lipodystrophy
  • Visceral abdominal fat
  • Body composition
  • HIV-associated NAFLD / MASLD
Tirzepatide distinctions
  • Obesity
  • Type 2 diabetes
  • Cardiometabolic outcomes
Research confidence by questionCompare regulatory, human-evidence, outcome, and administration records side by side.

Question by question

What each evidence base can actually answer

Reviewed July 25, 2026
Regulatory statusEvidence, not a winner
TesamorelinFDA approved for a defined indication

FDA approved for a defined indication

TirzepatideFDA-labeled indications

FDA approved as Mounjaro for type 2 diabetes and Zepbound for defined adult weight-management and OSA indications.

Evidence depthEvidence, not a winner
TesamorelinProfile in progress

Two randomized Phase 3 trials enrolling 816 adults with HIV-associated abdominal fat accumulation.

TirzepatideMature Phase 3

Multiple large Phase 3 trials, active-comparator studies, 176-week follow-up, a 13,299-participant cardiovascular outcomes trial, and newer 2026 maintenance data.

Weight outcomesEvidence, not a winner
TesamorelinRecord incomplete

No dedicated weight-outcome summary has been editorially approved.

TirzepatidePeer-reviewed Phase 3

SURMOUNT-1 peer-reviewed trial: mean change −15.0%, −19.5%, and −20.9% across studied doses versus −3.1% placebo at 72 weeks.

Type 2 diabetesEvidence, not a winner
TesamorelinRecord incomplete

No dedicated diabetes-outcome summary has been editorially approved.

TirzepatideApproved + Phase 3

Extensive SURPASS program and FDA approval. SURPASS-2 directly compared tirzepatide with semaglutide 1 mg in type 2 diabetes.

Obstructive sleep apnoeaEvidence, not a winner
TesamorelinRecord incomplete

No dedicated obstructive-sleep-apnoea outcome summary has been editorially approved.

TirzepatideApproved + Phase 3

Two peer-reviewed Phase 3 trials support the FDA-approved Zepbound indication for moderate-to-severe OSA in adults with obesity.

Cardiovascular outcomesEvidence, not a winner
TesamorelinRecord incomplete

No dedicated cardiovascular-outcome summary has been editorially approved.

TirzepatideCVOT + HFpEF trial

SURPASS-CVOT found tirzepatide noninferior—but not superior—to dulaglutide for major cardiovascular events. In SUMMIT, a separate placebo-controlled HFpEF-and-obesity population had fewer composite cardiovascular-death or worsening-heart-failure events; that finding is population-specific.

Administration and handlingEvidence, not a winner
TesamorelinOpen profile

Open the compound profile for approved-label information or clearly identified trial-administration records.

TirzepatideOfficial FDA label

FDA labels provide product-specific once-weekly subcutaneous dosing and handling. Approved presentations are solutions; no reconstitution is required.

Comparison limitationsUnderstand what this comparison cannot establish before interpreting separate studies.

Very limited comparison

  • No direct head-to-head trial is represented for this pair.
  • Separate studies may use different populations, endpoints, durations, doses, routes, and estimands.
  • Results should not be interpreted as comparative superiority or individual guidance.

Current unknowns

Questions the evidence cannot answer yet

Tesamorelin
  • Long-term cardiovascular safety and whether findings translate beyond the narrow populations studied.
Tirzepatide
  • Long-term individual durability and rare events, plus evidence for uses outside studied and approved populations.

Community Intelligence

Emerging patterns, clearly separated from evidence

Structured, approved self-reports only

Tesamorelin

No community experiences yetBe the first account holder to contribute.

Tirzepatide

No community experiences yetBe the first account holder to contribute.

Community Intelligence summarizes structured, self-reported experiences. It can reveal patterns and useful research questions, but it cannot prove safety, effectiveness, or cause and effect. Published evidence is always shown separately.