Mito Health: Helping you live healthier, longer.
In-depth bloodwork & holistic health advice, backed by the latest longevity science. Only $399.
When the Scale Stalls: Breaking Through a GLP‑1 Plateau
GLP-1 therapies often stall after initial weight loss; plateaus stem from physiology, dosing and behavior. This article explains causes, adjustments, and biomarkers to guide steps.

Written by
Mito Team

Understanding the GLP-1 plateau: why progress can slow and what to do
GLP-1 receptor agonists (GLP-1 RAs) such as semaglutide have changed treatment for obesity and type 2 diabetes by reducing appetite and caloric intake. Many people see rapid early weight loss followed by a slowing or pause in progress — commonly referred to as a GLP-1 plateau. This article explains likely causes, measurable signals to watch, practical adjustments that can restart momentum, and important safety considerations.
What a GLP-1 plateau usually means
A plateau often reflects a new energy balance rather than treatment failure. Reduced calorie intake lowers body weight, and the body responds by lowering energy expenditure and increasing appetite signals. These physiologic adaptations make continued weight loss harder even while on medication.
Plateaus are common across weight-loss approaches and can last weeks to months. Expecting steady linear loss is unrealistic; instead, look for longer-term trends in weight and metabolic markers.
Common drivers of a plateau on GLP‑1 therapy
Reduced resting metabolic rate and total daily energy expenditure after initial weight loss.
Loss of lean mass if protein intake and resistance training are inadequate.
Behavioral drift: smaller portion control lapses or reduced activity offsetting calorie gaps.
Dose-related effects: some formulations or doses reach maximal appetite suppression, so further dose increases—or different agents—may be considered with a prescriber.
Underlying medical issues (thyroid disease, medications) that alter metabolism.
How to interpret key biomarkers
Weight trend
Track weekly weights (same time, similar clothing) and focus on 4–12 week trends rather than day-to-day changes.
A stable or slowly rising trend suggests energy balance has shifted and may require behavioral or medical adjustments.
Resting heart rate
A rising resting heart rate can indicate increased stress, dehydration, or inadequate recovery; it may accompany catabolic states.
Small, sustained changes warrant attention and possibly clinical review.
HbA1c
For people with diabetes, HbA1c shows glycemic control and metabolic response to therapy. Plateaus in weight can occur independently of improvements in HbA1c, but both are useful outcomes to monitor.
Practical, evidence‑informed strategies to move past a plateau
Adjust expectations first. Plateaus are common and often signal a new baseline. Small, sustainable changes usually work better than extremes.
Nutrition
Prioritize protein to preserve lean mass; aim to include a protein source at each meal. Exact targets vary; discuss individualized goals with a clinician or dietitian.
Avoid crash dieting. Very low-calorie approaches can accelerate lean mass loss and worsen metabolic adaptation.
Focus on nutrient-dense foods and portion awareness rather than rigid elimination.
Activity and strength training
Add or increase resistance training 2–3 times per week to protect or rebuild muscle, which supports resting metabolic rate.
Increase non-exercise activity thermogenesis (NEAT): more steps, standing breaks, household movement.
Sleep and stress
Improve sleep duration and quality; poor sleep can increase appetite and blunt weight-loss responses.
Address chronic stress with behavioral strategies; stress hormones can influence appetite and energy storage.
Behavioral and monitoring tweaks
Revisit meal timing, record food intake for short periods to identify drift, and set measurable activity goals.
Use the weight trend, resting heart rate, and HbA1c to assess whether adjustments are having metabolic effects.
Medication and dose strategy
Dose changes or switching agents may help some people, but any changes must be made with the prescriber. For semaglutide:
Clinical products for weight (e.g., Wegovy) follow a weekly escalation to higher maintenance doses than diabetes formulations (e.g., Ozempic).
Oral semaglutide (Rybelsus) differs in formulation and dosing from injectable semaglutide; absorption and side-effect profiles vary.
Some alternative agents (e.g., tirzepatide, a GIP/GLP-1 agonist) have shown greater average weight loss in trials, but suitability depends on individual health factors and prescriber assessment.
Safety notes, contraindications, and who should avoid GLP‑1 adjustments without medical review
Never make dose changes without consulting the prescriber. Escalation increases both efficacy and side effects.
Avoid crash diets and extreme caloric restriction; these can cause harm and counterproductive metabolic effects.
People with a personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 (MEN2) are generally advised against GLP‑1 RAs; discuss family history with your clinician.
Use caution and close monitoring if taking insulin or insulin secretagogues (e.g., sulfonylureas) because of hypoglycemia risk when calories fall.
Prior pancreatitis, severe gastrointestinal disease, pregnancy, and breastfeeding are situations where GLP‑1 therapy may be contraindicated or require careful review.
Watch for persistent severe gastrointestinal side effects; dose changes or switching agents may be needed under supervision.
When to seek clinical re-evaluation
If weight plateaus for several months despite adherence to behavioral adjustments.
If you notice concerning biomarker shifts (sustained rise in resting heart rate, worsening HbA1c, or unexplained weight gain).
If side effects limit adherence or quality of life.
For assessment of alternate pharmacologic options, combination strategies, or the need for additional diagnostic testing.
Takeaways and practical next steps
A GLP-1 plateau is often a sign of a new energy balance and is common; it does not necessarily mean the therapy has failed.
Small, sustainable changes—more protein, resistance training, increased NEAT, better sleep, and behavioral refinements—are first-line approaches to restart progress.
Monitor weight trends, resting heart rate, and HbA1c to guide adjustments and to detect issues early.
Do not crash-diet. Discuss any dose changes, switching agents, or medication additions with your prescriber, especially if you take insulin or have relevant medical history.
Conclusion
Plateaus on GLP‑1 therapy, including weight loss plateau on semaglutide, are expected and manageable for many people. Combining careful monitoring of biomarkers with evidence‑based dietary, activity, and sleep strategies—and consulting your care team about medication options—helps align expectations and supports safe, sustainable progress.
Join Mito to test 100+ biomarkers and get concierge-level guidance from your care team
Mito Health: Helping you live healthier, longer.
In-depth bloodwork & holistic health advice, backed by the latest longevity science. Only $399.
When the Scale Stalls: Breaking Through a GLP‑1 Plateau
GLP-1 therapies often stall after initial weight loss; plateaus stem from physiology, dosing and behavior. This article explains causes, adjustments, and biomarkers to guide steps.

Written by
Mito Team

Understanding the GLP-1 plateau: why progress can slow and what to do
GLP-1 receptor agonists (GLP-1 RAs) such as semaglutide have changed treatment for obesity and type 2 diabetes by reducing appetite and caloric intake. Many people see rapid early weight loss followed by a slowing or pause in progress — commonly referred to as a GLP-1 plateau. This article explains likely causes, measurable signals to watch, practical adjustments that can restart momentum, and important safety considerations.
What a GLP-1 plateau usually means
A plateau often reflects a new energy balance rather than treatment failure. Reduced calorie intake lowers body weight, and the body responds by lowering energy expenditure and increasing appetite signals. These physiologic adaptations make continued weight loss harder even while on medication.
Plateaus are common across weight-loss approaches and can last weeks to months. Expecting steady linear loss is unrealistic; instead, look for longer-term trends in weight and metabolic markers.
Common drivers of a plateau on GLP‑1 therapy
Reduced resting metabolic rate and total daily energy expenditure after initial weight loss.
Loss of lean mass if protein intake and resistance training are inadequate.
Behavioral drift: smaller portion control lapses or reduced activity offsetting calorie gaps.
Dose-related effects: some formulations or doses reach maximal appetite suppression, so further dose increases—or different agents—may be considered with a prescriber.
Underlying medical issues (thyroid disease, medications) that alter metabolism.
How to interpret key biomarkers
Weight trend
Track weekly weights (same time, similar clothing) and focus on 4–12 week trends rather than day-to-day changes.
A stable or slowly rising trend suggests energy balance has shifted and may require behavioral or medical adjustments.
Resting heart rate
A rising resting heart rate can indicate increased stress, dehydration, or inadequate recovery; it may accompany catabolic states.
Small, sustained changes warrant attention and possibly clinical review.
HbA1c
For people with diabetes, HbA1c shows glycemic control and metabolic response to therapy. Plateaus in weight can occur independently of improvements in HbA1c, but both are useful outcomes to monitor.
Practical, evidence‑informed strategies to move past a plateau
Adjust expectations first. Plateaus are common and often signal a new baseline. Small, sustainable changes usually work better than extremes.
Nutrition
Prioritize protein to preserve lean mass; aim to include a protein source at each meal. Exact targets vary; discuss individualized goals with a clinician or dietitian.
Avoid crash dieting. Very low-calorie approaches can accelerate lean mass loss and worsen metabolic adaptation.
Focus on nutrient-dense foods and portion awareness rather than rigid elimination.
Activity and strength training
Add or increase resistance training 2–3 times per week to protect or rebuild muscle, which supports resting metabolic rate.
Increase non-exercise activity thermogenesis (NEAT): more steps, standing breaks, household movement.
Sleep and stress
Improve sleep duration and quality; poor sleep can increase appetite and blunt weight-loss responses.
Address chronic stress with behavioral strategies; stress hormones can influence appetite and energy storage.
Behavioral and monitoring tweaks
Revisit meal timing, record food intake for short periods to identify drift, and set measurable activity goals.
Use the weight trend, resting heart rate, and HbA1c to assess whether adjustments are having metabolic effects.
Medication and dose strategy
Dose changes or switching agents may help some people, but any changes must be made with the prescriber. For semaglutide:
Clinical products for weight (e.g., Wegovy) follow a weekly escalation to higher maintenance doses than diabetes formulations (e.g., Ozempic).
Oral semaglutide (Rybelsus) differs in formulation and dosing from injectable semaglutide; absorption and side-effect profiles vary.
Some alternative agents (e.g., tirzepatide, a GIP/GLP-1 agonist) have shown greater average weight loss in trials, but suitability depends on individual health factors and prescriber assessment.
Safety notes, contraindications, and who should avoid GLP‑1 adjustments without medical review
Never make dose changes without consulting the prescriber. Escalation increases both efficacy and side effects.
Avoid crash diets and extreme caloric restriction; these can cause harm and counterproductive metabolic effects.
People with a personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 (MEN2) are generally advised against GLP‑1 RAs; discuss family history with your clinician.
Use caution and close monitoring if taking insulin or insulin secretagogues (e.g., sulfonylureas) because of hypoglycemia risk when calories fall.
Prior pancreatitis, severe gastrointestinal disease, pregnancy, and breastfeeding are situations where GLP‑1 therapy may be contraindicated or require careful review.
Watch for persistent severe gastrointestinal side effects; dose changes or switching agents may be needed under supervision.
When to seek clinical re-evaluation
If weight plateaus for several months despite adherence to behavioral adjustments.
If you notice concerning biomarker shifts (sustained rise in resting heart rate, worsening HbA1c, or unexplained weight gain).
If side effects limit adherence or quality of life.
For assessment of alternate pharmacologic options, combination strategies, or the need for additional diagnostic testing.
Takeaways and practical next steps
A GLP-1 plateau is often a sign of a new energy balance and is common; it does not necessarily mean the therapy has failed.
Small, sustainable changes—more protein, resistance training, increased NEAT, better sleep, and behavioral refinements—are first-line approaches to restart progress.
Monitor weight trends, resting heart rate, and HbA1c to guide adjustments and to detect issues early.
Do not crash-diet. Discuss any dose changes, switching agents, or medication additions with your prescriber, especially if you take insulin or have relevant medical history.
Conclusion
Plateaus on GLP‑1 therapy, including weight loss plateau on semaglutide, are expected and manageable for many people. Combining careful monitoring of biomarkers with evidence‑based dietary, activity, and sleep strategies—and consulting your care team about medication options—helps align expectations and supports safe, sustainable progress.
Join Mito to test 100+ biomarkers and get concierge-level guidance from your care team
Mito Health: Helping you live healthier, longer.
In-depth bloodwork & holistic health advice, backed by the latest longevity science. Only $399.
When the Scale Stalls: Breaking Through a GLP‑1 Plateau
GLP-1 therapies often stall after initial weight loss; plateaus stem from physiology, dosing and behavior. This article explains causes, adjustments, and biomarkers to guide steps.

Written by
Mito Team

Understanding the GLP-1 plateau: why progress can slow and what to do
GLP-1 receptor agonists (GLP-1 RAs) such as semaglutide have changed treatment for obesity and type 2 diabetes by reducing appetite and caloric intake. Many people see rapid early weight loss followed by a slowing or pause in progress — commonly referred to as a GLP-1 plateau. This article explains likely causes, measurable signals to watch, practical adjustments that can restart momentum, and important safety considerations.
What a GLP-1 plateau usually means
A plateau often reflects a new energy balance rather than treatment failure. Reduced calorie intake lowers body weight, and the body responds by lowering energy expenditure and increasing appetite signals. These physiologic adaptations make continued weight loss harder even while on medication.
Plateaus are common across weight-loss approaches and can last weeks to months. Expecting steady linear loss is unrealistic; instead, look for longer-term trends in weight and metabolic markers.
Common drivers of a plateau on GLP‑1 therapy
Reduced resting metabolic rate and total daily energy expenditure after initial weight loss.
Loss of lean mass if protein intake and resistance training are inadequate.
Behavioral drift: smaller portion control lapses or reduced activity offsetting calorie gaps.
Dose-related effects: some formulations or doses reach maximal appetite suppression, so further dose increases—or different agents—may be considered with a prescriber.
Underlying medical issues (thyroid disease, medications) that alter metabolism.
How to interpret key biomarkers
Weight trend
Track weekly weights (same time, similar clothing) and focus on 4–12 week trends rather than day-to-day changes.
A stable or slowly rising trend suggests energy balance has shifted and may require behavioral or medical adjustments.
Resting heart rate
A rising resting heart rate can indicate increased stress, dehydration, or inadequate recovery; it may accompany catabolic states.
Small, sustained changes warrant attention and possibly clinical review.
HbA1c
For people with diabetes, HbA1c shows glycemic control and metabolic response to therapy. Plateaus in weight can occur independently of improvements in HbA1c, but both are useful outcomes to monitor.
Practical, evidence‑informed strategies to move past a plateau
Adjust expectations first. Plateaus are common and often signal a new baseline. Small, sustainable changes usually work better than extremes.
Nutrition
Prioritize protein to preserve lean mass; aim to include a protein source at each meal. Exact targets vary; discuss individualized goals with a clinician or dietitian.
Avoid crash dieting. Very low-calorie approaches can accelerate lean mass loss and worsen metabolic adaptation.
Focus on nutrient-dense foods and portion awareness rather than rigid elimination.
Activity and strength training
Add or increase resistance training 2–3 times per week to protect or rebuild muscle, which supports resting metabolic rate.
Increase non-exercise activity thermogenesis (NEAT): more steps, standing breaks, household movement.
Sleep and stress
Improve sleep duration and quality; poor sleep can increase appetite and blunt weight-loss responses.
Address chronic stress with behavioral strategies; stress hormones can influence appetite and energy storage.
Behavioral and monitoring tweaks
Revisit meal timing, record food intake for short periods to identify drift, and set measurable activity goals.
Use the weight trend, resting heart rate, and HbA1c to assess whether adjustments are having metabolic effects.
Medication and dose strategy
Dose changes or switching agents may help some people, but any changes must be made with the prescriber. For semaglutide:
Clinical products for weight (e.g., Wegovy) follow a weekly escalation to higher maintenance doses than diabetes formulations (e.g., Ozempic).
Oral semaglutide (Rybelsus) differs in formulation and dosing from injectable semaglutide; absorption and side-effect profiles vary.
Some alternative agents (e.g., tirzepatide, a GIP/GLP-1 agonist) have shown greater average weight loss in trials, but suitability depends on individual health factors and prescriber assessment.
Safety notes, contraindications, and who should avoid GLP‑1 adjustments without medical review
Never make dose changes without consulting the prescriber. Escalation increases both efficacy and side effects.
Avoid crash diets and extreme caloric restriction; these can cause harm and counterproductive metabolic effects.
People with a personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 (MEN2) are generally advised against GLP‑1 RAs; discuss family history with your clinician.
Use caution and close monitoring if taking insulin or insulin secretagogues (e.g., sulfonylureas) because of hypoglycemia risk when calories fall.
Prior pancreatitis, severe gastrointestinal disease, pregnancy, and breastfeeding are situations where GLP‑1 therapy may be contraindicated or require careful review.
Watch for persistent severe gastrointestinal side effects; dose changes or switching agents may be needed under supervision.
When to seek clinical re-evaluation
If weight plateaus for several months despite adherence to behavioral adjustments.
If you notice concerning biomarker shifts (sustained rise in resting heart rate, worsening HbA1c, or unexplained weight gain).
If side effects limit adherence or quality of life.
For assessment of alternate pharmacologic options, combination strategies, or the need for additional diagnostic testing.
Takeaways and practical next steps
A GLP-1 plateau is often a sign of a new energy balance and is common; it does not necessarily mean the therapy has failed.
Small, sustainable changes—more protein, resistance training, increased NEAT, better sleep, and behavioral refinements—are first-line approaches to restart progress.
Monitor weight trends, resting heart rate, and HbA1c to guide adjustments and to detect issues early.
Do not crash-diet. Discuss any dose changes, switching agents, or medication additions with your prescriber, especially if you take insulin or have relevant medical history.
Conclusion
Plateaus on GLP‑1 therapy, including weight loss plateau on semaglutide, are expected and manageable for many people. Combining careful monitoring of biomarkers with evidence‑based dietary, activity, and sleep strategies—and consulting your care team about medication options—helps align expectations and supports safe, sustainable progress.
Join Mito to test 100+ biomarkers and get concierge-level guidance from your care team
When the Scale Stalls: Breaking Through a GLP‑1 Plateau
GLP-1 therapies often stall after initial weight loss; plateaus stem from physiology, dosing and behavior. This article explains causes, adjustments, and biomarkers to guide steps.

Written by
Mito Team

Understanding the GLP-1 plateau: why progress can slow and what to do
GLP-1 receptor agonists (GLP-1 RAs) such as semaglutide have changed treatment for obesity and type 2 diabetes by reducing appetite and caloric intake. Many people see rapid early weight loss followed by a slowing or pause in progress — commonly referred to as a GLP-1 plateau. This article explains likely causes, measurable signals to watch, practical adjustments that can restart momentum, and important safety considerations.
What a GLP-1 plateau usually means
A plateau often reflects a new energy balance rather than treatment failure. Reduced calorie intake lowers body weight, and the body responds by lowering energy expenditure and increasing appetite signals. These physiologic adaptations make continued weight loss harder even while on medication.
Plateaus are common across weight-loss approaches and can last weeks to months. Expecting steady linear loss is unrealistic; instead, look for longer-term trends in weight and metabolic markers.
Common drivers of a plateau on GLP‑1 therapy
Reduced resting metabolic rate and total daily energy expenditure after initial weight loss.
Loss of lean mass if protein intake and resistance training are inadequate.
Behavioral drift: smaller portion control lapses or reduced activity offsetting calorie gaps.
Dose-related effects: some formulations or doses reach maximal appetite suppression, so further dose increases—or different agents—may be considered with a prescriber.
Underlying medical issues (thyroid disease, medications) that alter metabolism.
How to interpret key biomarkers
Weight trend
Track weekly weights (same time, similar clothing) and focus on 4–12 week trends rather than day-to-day changes.
A stable or slowly rising trend suggests energy balance has shifted and may require behavioral or medical adjustments.
Resting heart rate
A rising resting heart rate can indicate increased stress, dehydration, or inadequate recovery; it may accompany catabolic states.
Small, sustained changes warrant attention and possibly clinical review.
HbA1c
For people with diabetes, HbA1c shows glycemic control and metabolic response to therapy. Plateaus in weight can occur independently of improvements in HbA1c, but both are useful outcomes to monitor.
Practical, evidence‑informed strategies to move past a plateau
Adjust expectations first. Plateaus are common and often signal a new baseline. Small, sustainable changes usually work better than extremes.
Nutrition
Prioritize protein to preserve lean mass; aim to include a protein source at each meal. Exact targets vary; discuss individualized goals with a clinician or dietitian.
Avoid crash dieting. Very low-calorie approaches can accelerate lean mass loss and worsen metabolic adaptation.
Focus on nutrient-dense foods and portion awareness rather than rigid elimination.
Activity and strength training
Add or increase resistance training 2–3 times per week to protect or rebuild muscle, which supports resting metabolic rate.
Increase non-exercise activity thermogenesis (NEAT): more steps, standing breaks, household movement.
Sleep and stress
Improve sleep duration and quality; poor sleep can increase appetite and blunt weight-loss responses.
Address chronic stress with behavioral strategies; stress hormones can influence appetite and energy storage.
Behavioral and monitoring tweaks
Revisit meal timing, record food intake for short periods to identify drift, and set measurable activity goals.
Use the weight trend, resting heart rate, and HbA1c to assess whether adjustments are having metabolic effects.
Medication and dose strategy
Dose changes or switching agents may help some people, but any changes must be made with the prescriber. For semaglutide:
Clinical products for weight (e.g., Wegovy) follow a weekly escalation to higher maintenance doses than diabetes formulations (e.g., Ozempic).
Oral semaglutide (Rybelsus) differs in formulation and dosing from injectable semaglutide; absorption and side-effect profiles vary.
Some alternative agents (e.g., tirzepatide, a GIP/GLP-1 agonist) have shown greater average weight loss in trials, but suitability depends on individual health factors and prescriber assessment.
Safety notes, contraindications, and who should avoid GLP‑1 adjustments without medical review
Never make dose changes without consulting the prescriber. Escalation increases both efficacy and side effects.
Avoid crash diets and extreme caloric restriction; these can cause harm and counterproductive metabolic effects.
People with a personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 (MEN2) are generally advised against GLP‑1 RAs; discuss family history with your clinician.
Use caution and close monitoring if taking insulin or insulin secretagogues (e.g., sulfonylureas) because of hypoglycemia risk when calories fall.
Prior pancreatitis, severe gastrointestinal disease, pregnancy, and breastfeeding are situations where GLP‑1 therapy may be contraindicated or require careful review.
Watch for persistent severe gastrointestinal side effects; dose changes or switching agents may be needed under supervision.
When to seek clinical re-evaluation
If weight plateaus for several months despite adherence to behavioral adjustments.
If you notice concerning biomarker shifts (sustained rise in resting heart rate, worsening HbA1c, or unexplained weight gain).
If side effects limit adherence or quality of life.
For assessment of alternate pharmacologic options, combination strategies, or the need for additional diagnostic testing.
Takeaways and practical next steps
A GLP-1 plateau is often a sign of a new energy balance and is common; it does not necessarily mean the therapy has failed.
Small, sustainable changes—more protein, resistance training, increased NEAT, better sleep, and behavioral refinements—are first-line approaches to restart progress.
Monitor weight trends, resting heart rate, and HbA1c to guide adjustments and to detect issues early.
Do not crash-diet. Discuss any dose changes, switching agents, or medication additions with your prescriber, especially if you take insulin or have relevant medical history.
Conclusion
Plateaus on GLP‑1 therapy, including weight loss plateau on semaglutide, are expected and manageable for many people. Combining careful monitoring of biomarkers with evidence‑based dietary, activity, and sleep strategies—and consulting your care team about medication options—helps align expectations and supports safe, sustainable progress.
Join Mito to test 100+ biomarkers and get concierge-level guidance from your care team
Mito Health: Helping you live healthier, longer.
In-depth bloodwork & holistic health advice, backed by the latest longevity science. Only $399.
Recently published
What could cost you $15,000? $349 with Mito.
No hidden fees. No subscription traps. Just real care.
What's included
Core Test - Comprehensive lab test covering 100+ biomarkers
Clinician reviewed insights and action plan
1:1 consultation with a real clinician
Upload past lab reports for lifetime tracking
Dedicated 1:1 health coaching
Duo Bundle (For 2)
Most popular
$798
$668
$130 off (17%)
Individual
$399
$349
$50 off (13%)
What could cost you $15,000? $349 with Mito.
No hidden fees. No subscription traps. Just real care.
What's included
Core Test - Comprehensive lab test covering 100+ biomarkers
Clinician reviewed insights and action plan
1:1 consultation with a real clinician
Upload past lab reports for lifetime tracking
Dedicated 1:1 health coaching
Duo Bundle (For 2)
Most popular
$798
$668
$130 off (17%)
Individual
$399
$349
$50 off (13%)
What could cost you $15,000? $349 with Mito.
No hidden fees. No subscription traps. Just real care.
What's included
Core Test - Comprehensive lab test covering 100+ biomarkers
Clinician reviewed insights and action plan
1:1 consultation with a real clinician
Upload past lab reports for lifetime tracking
Dedicated 1:1 health coaching
Duo Bundle (For 2)
Most popular
$798
$668
$130 off (17%)
Individual
$399
$349
$50 off (13%)
What could cost you $15,000? $349 with Mito.
No hidden fees. No subscription traps. Just real care.
Core Test - Comprehensive lab test covering 100+ biomarkers
Clinician reviewed insights and action plan
1:1 consultation with a real clinician
Upload past lab reports for lifetime tracking
Dedicated 1:1 health coaching
What's included
Duo Bundle (For 2)
Most popular
$798
$668
$130 off (17%)
Individual
$399
$349
$50 off (13%)


