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Chapter 7 

Part 4 – Tirzepatide & Future Therapies

Retatrutide & Triple-Agonist Therapies: The Next Frontier

Researchers are studying medications that target three metabolic pathways at once. Here’s what’s investigational, what’s real, and what it means for the future of obesity care.

FDA

regulated medications

8

chapters in this guide

Physician-Reviewed

Medical Weight Loss Guide

KEY TAKEAWAY

Obesity medicine continues to evolve at an extraordinary pace. While GLP-1 receptor agonists such as Semaglutide and dual-agonist therapies such as Tirzepatide have transformed treatment, researchers are now studying a new generation of medications designed to target three metabolic pathways simultaneously. These investigational therapies remain under clinical investigation and are not yet approved by the FDA for clinical use.

A new generation of medicines

The approval of Semaglutide marked a turning point in obesity medicine. Tirzepatide expanded that progress by activating two naturally occurring metabolic pathways instead of one. Today, researchers are exploring whether activating three complementary hormone pathways simultaneously may produce additional metabolic benefits — building upon, rather than replacing, earlier medications.

What is Retatrutide?

Retatrutide is an investigational medication currently being studied in clinical trials, designed to activate three metabolic pathways: GLP-1, GIP, and glucagon. Researchers are studying whether activating these pathways together may provide complementary metabolic effects. As of publication, Retatrutide remains investigational and has not been approved by the FDA — clinical trials are ongoing.

Why add glucagon?

Many people associate glucagon only with blood sugar regulation. Researchers have also been studying its potential role in energy expenditure, fat metabolism, and metabolic flexibility. Scientists hope combining glucagon receptor activity with GLP-1 and GIP may create therapies that more closely mimic the body’s complex hormonal network — more research is still needed.

Beyond medications: personalization

The future of obesity care is not only about newer drugs — it’s about better personalization. Future treatment plans may consider genetics, biomarkers, laboratory testing, body composition, sleep, stress, wearable data, and treatment response. Instead of asking “what medication treats obesity,” providers may increasingly ask “what treatment works best for this individual?”

Oral GLP-1 medications

Another exciting area of research involves oral formulations, since many patients prefer taking medication by mouth rather than using injections. Researchers continue developing newer oral GLP-1 therapies designed to improve convenience while maintaining effectiveness; several investigational medications remain in clinical development.

Technology is transforming care

Modern obesity medicine extends beyond medication — mobile health apps, connected scales, laboratory integration, continuous glucose monitoring, wearable devices, AI-assisted education, and remote monitoring help patients stay engaged while giving providers additional information. Technology should enhance, not replace, the relationship between patients and clinicians.

Clinical Pearl

The future of obesity medicine is likely to become increasingly personalized. Rather than every patient receiving the same treatment, healthcare providers may use clinical data, laboratory testing, biomarkers, and ongoing treatment response to individualize care over time.
What I appreciated most was that my provider didn’t push me toward the newest option just because it was newest. We talked through what actually made sense for me, and that made me trust the plan a lot more.
— He & She MD patient. Individual experiences vary.

Myth vs. Fact

Myth: “The newest medication is always the best.”
Fact: The most appropriate treatment depends on an individual’s medical history, goals, preferences, response to therapy, and healthcare provider’s clinical judgment.

Myth: “Future technology will replace doctors.”
Fact: Technology can improve communication, monitoring, and education, but it is intended to support — not replace — the expertise of licensed healthcare professionals.

Research Spotlight

A Phase 2 trial of Retatrutide published in the New England Journal of Medicine found that the investigational triple-hormone-receptor agonist produced dose-dependent reductions in body weight among adults with obesity. Retatrutide remains under clinical investigation and is not yet FDA-approved.

Frequently Asked Questions

Is Retatrutide FDA-approved?

No. Retatrutide is an investigational medication that has not been approved by the FDA. Clinical trials are ongoing.

A medication designed to activate three metabolic pathways at once — GLP-1, GIP, and glucagon — rather than one or two.

No. Digital tools are designed to support — not replace — the relationship between patients and licensed healthcare providers.

Ongoing research helps scientists better understand how appetite and metabolism are regulated, which may lead to additional treatment options for appropriate patients in the future.

Scientific References

  1. Jastreboff AM, et al. Triple–Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial. N Engl J Med. 2023. Read source
  2. Eli Lilly and Company — Phase 2 Retatrutide Results Published in NEJM. Read source

Disclaimers

Retatrutide is not currently FDA-approved and is not available through He & She MD. This chapter is provided for educational purposes only, based on published clinical research. We do not prescribe or dispense retatrutide.

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