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💊 Pharma Partnerships · GLP-1 & Metabolic Therapies

Turn Your GLP-1 Patients
Into the Real-World Evidence
Your Pipeline Needs.

30–50% of GLP-1 patients discontinue within six months. Every one of them is a lost outcome, a lost data point, and a lost story. SureMediks closes the gap between visits — extending adherence, capturing real-world evidence, and giving your medical affairs and commercial teams the longitudinal patient journey your clinical trials never could.

Pharmaceutical Research
📈
2–3×
Adherence vs.
standard of care
🔬
BHB
Direct fat-metabolism
RWE asset
30–50%
Drop-Off Window
First 6 months on GLP-1 therapy
2–3×
Adherence Lift
vs. unstructured programmes
12–18 mo
Patient Lifecycle
Continuous longitudinal capture
RWE
Pipeline-Ready Data
Adherence · outcomes · PROs
Springer Nature · Peer-reviewed in Obesity Surgery
·
391 trial participants · multinational
·
HIPAA · GxP-aligned · 21 CFR Part 11 ready
·
Realistic Intelligence® · Registered AI engine
·
BHB Ketone · Direct fat-metabolism RWE
📈 The Evidence Asset Hiding Inside Your Therapy

25–40% of GLP-1 Weight Loss Can Be Muscle. The Brand That Captures & Preserves It Wins the Long Game.

Body-composition outcomes — including direct fat-metabolism data — are the next frontier of GLP-1 differentiation. Pharma medical affairs teams know it. Payers are starting to ask about it. Most patient support programmes can't capture either signal at scale. SureMediks turns the lean-mass and fat-metabolism questions from clinical concerns into a publishable, payer-ready evidence asset for your therapy.

⚖️
Body Composition + Direct Fat-Metabolism Data, at Population Scale
SureMediks Smart Scale + Ketone Meter · structured longitudinal capture · every patient

SureMediks generates the dataset clinical trials cannot: weekly body composition (weight, body-fat percentage, lean muscle) plus on-demand BHB ketone readings — the only direct circulating biomarker for fat metabolism. Together, these turn your therapy's body-composition story from inferred to measured.

  • Weekly lean mass trajectories across thousands of patients on your therapy
  • BHB ketone data — direct evidence of fat metabolism your trials never captured at this scale
  • Comparative body composition cohorts against historical or competitor benchmarks
  • Sub-population analyses — older patients, perimenopausal women, frail and at-risk groups
  • Publication-ready datasets for medical affairs, advisory boards, and payer evidence
🥗
Nutrition as a Therapy Extender
SureMediks Nutrition Module · structured · protocol-driven · patient-engaged

GLP-1 patients eat dramatically less. The SureMediks nutrition manager actively preserves muscle and engagement — turning your therapy from a weight-loss intervention into a coordinated body-composition outcome.

  • Protein targets at 1.2–1.6 g/kg ideal body weight — the clinical lever for muscle preservation
  • Daily intake tracking with structured PRO capture
  • Provider-coded meal protocols aligned to your therapy's profile
  • Hydration and electrolyte data across the GI tolerance window
  • Engagement and adherence signals that strengthen your real-world outcomes story
25–40%
Of GLP-1 Weight Loss
Can be lean muscle mass — your therapy's hidden differentiator
Weekly
Body Composition Capture
Continuous longitudinal data across the entire cohort
BHB + Composition
Publication-Ready RWE
Direct fat-metabolism + body composition · datasets your trials cannot replicate
Interactive Walkthrough

See Exactly How SureMediks Extends Your Therapy.

Click any phase below to see the modules, the data captured, and what Realistic Intelligence® does — through whichever lens matters to your team.

📊
Commercial & Brand Teams
Adherence as a measurable lift on top of your therapy.
Patients stay on therapy longer. Refills compound. The clinical case for your brand strengthens with every retained patient. White-label deployment available.
🔬
Medical Affairs
Patient support programmes that actually move outcomes.
Provider-coded protocols, structured behavioral support, validated PROs. The kind of support programme medical affairs teams want to defend at advisory boards.
📈
Real-World Evidence & HEOR
The longitudinal patient journey your trials can't capture.
Continuous, patient-consented data: weight trajectories, adherence patterns, comorbidity progression, PROs. Pipeline-ready for RWE publications and payer evidence.
      ⚡ Realistic Intelligence® at this phase
      💊 Pharma value delivered
      For Commercial & Brand
      For Medical Affairs
      For RWE & HEOR
      Phase 1 of 6
      ⚡ One Patient. Six Months. The Difference SureMediks Makes for Your Brand.
      Take a 47-year-old patient on your GLP-1 therapy.
      Day 14. Her nausea spikes. She stops eating. She doesn't call the clinic — she figures she'll mention it at her next visit, three weeks away.

      Without SureMediks: she silently discontinues by Day 21. She tells her friends the medication "didn't work for her." Her data never enters your post-marketing dataset. She becomes part of the 30–50% statistic that follows your therapy in every market access conversation.

      With SureMediks: her tolerance signal routes through Realistic Intelligence®, the coach gets the alert within hours, the dose is paused and a hydration protocol is delivered through the patient app. By Day 25 she's titrating again. She stays on therapy through month 6, month 12, month 18 — generating the kind of longitudinal real-world evidence your medical affairs team can publish, your commercial team can cite, and your HEOR team can present to payers.

      This is what "extending therapy beyond the prescription" actually looks like.
      Realistic Intelligence® in action
      Why Pharma Partners Choose SureMediks

      More Than a Patient Support
      Programme. A Real-World
      Evidence Engine.

      Most pharma-funded support programmes are call centres with apps bolted on. SureMediks is a clinical-grade platform that extends your therapy, captures the data your pipeline needs, and meets the regulatory bar your medical affairs team requires.

      • White-label deployment under your brand or co-branded
      • 21 CFR Part 11 and GxP-aligned data capture
      • Validated patient-reported outcomes (PROs) at scale
      • Realistic Intelligence® — provider-coded protocols, not generic AI
      • Continuous longitudinal data — adherence, weight, comorbidities, PROs
      • Publication-ready datasets for medical affairs and HEOR
      • Privacy-first architecture · HIPAA · patient-consented
      Schedule a Partnership Call →
      Pharma Research Lab
      Next Step

      Let's Map This Onto Your Therapy.

      A 30-minute partnership call to map this six-phase walkthrough onto your therapy, your indication, your medical affairs strategy and your real-world evidence priorities. No pitch deck. A conversation between people who care about extending therapy beyond the prescription.