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The research behind every active.

ProleevaMax pairs thirteen standardized actives across six pathways of the inflammatory response. Here is the published science on each one — the effect sizes, the sample sizes, and the journals, with a link to every study.

peer-reviewed studies
28

peer-reviewed studies

inflammatory pathways
6

inflammatory pathways

standardized actives
13

standardized actives

Meta-analysisOsteoarthritis

−8.33 pts

Pain (VAS, 0–100) · p < 0.00001

-15fewer ←2

Pooled across 7 trials, boswellia lowered pain on the visual-analog scale and improved WOMAC pain (−14.22) and stiffness.

7 RCTs · 545 participants · ≥ 4 weeks

BMC Complementary Medicine and Therapies, 2020

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Boswellia Serrata — raw ingredient

Ingredient

Boswellia serrata

RCTKnee osteoarthritis

Cartilage ↑

Knee cartilage (MRI) · p < 0.001

A 180-day MRI trial measured increased cartilage volume, thickness and joint-space width versus placebo, alongside lower hsCRP, MMP-3 and CTX-II.

80 participants · 180 days

Journal of the American Nutrition Association, 2025

Read the study
Boswellia Serrata — raw ingredient

Ingredient

Boswellia (Aflapin)

RCTKnee osteoarthritis

−44.4%

WOMAC pain · significant vs placebo

-100fewer ←0

Over 30 days, WOMAC pain fell 44.4% and VAS pain 45%, with reductions in MMP-3, TNF-α and hsCRP.

70 participants · 30 days

Journal of the American Nutrition Association, 2023

Read the study
Boswellia Serrata — raw ingredient

Ingredient

Boswellia (Aflapin)

Meta-analysisRheumatoid arthritis

−1.20 DAS28

Disease activity (DAS28) · p = 0.0003

-2fewer ←0.4

Curcumin lowered rheumatoid disease-activity scores and ESR (−29.47), with fewer swollen and tender joints.

6 studies · 539 participants · pooled

Frontiers in Immunology, 2023

Read the study
Curcumin — raw ingredient

Ingredient

Curcumin

Meta-analysisArthritis

Improved

Arthritis pain & inflammation · across 5 arthritis types

The largest pooled curcumin analysis to date — across nearly 2,400 participants and five arthritis types — found consistent improvement in pain and inflammatory markers.

29 RCTs · 2,396 participants · 4–36 weeks

Frontiers in Immunology, 2022

Read the study
Curcumin — raw ingredient

Ingredient

Curcumin

Meta-analysisMetabolic syndrome

−0.55 SMD

CRP (SMD) · p < 0.001

-1.2fewer ←0.4

Pooled across 24 trials, resveratrol lowered C-reactive protein (CRP) and TNF-α (SMD −0.68) — two core inflammatory markers.

24 RCTs · pooled

Food & Function, 2018

Read the study
Resveratrol — raw ingredient

Ingredient

Resveratrol

RCTIBS-D (post-infectious)

79.6% vs 5.8%

Responder rate · p < 0.0001

Placebo 5.8%→ more100

Glutamine normalized intestinal permeability: 79.6% of participants responded versus 5.8% on placebo, with symptom scores nearly halving.

106 participants · 8 weeks

Gut, 2019

Read the study
L-Glutamine — raw ingredient

Ingredient

L-Glutamine

RCTHSAN1 neuropathy

−1.5 units

Neuropathy score (CMTNS) · p = 0.03

-3fewer ←1

High-dose L-serine slowed neuropathy progression over a year and shifted the underlying sphingolipid profile.

18 participants · 1 year

Neurology, 2019

Read the study
L-Serine — raw ingredient

Ingredient

L-Serine

RCTCardiometabolic

Markers ↓

IL-6 & MCP-1 · p < 0.01

Six months of L-arginine lowered IL-6 and MCP-1 and improved insulin sensitivity and adiponectin.

64 participants · 6 months

Metabolism, 2009

Read the study
L-Arginine — raw ingredient

Ingredient

L-Arginine

RCTBioavailability

+2,000%

Curcumin bioavailability · landmark PK study

Co-administering piperine raised curcumin bioavailability by up to 2,000% in humans — the reason the two are paired.

Foundational pharmacokinetic citation; supports the delivery rationale, not a clinical outcome.

human crossover · pharmacokinetic

Planta Medica, 1998

Read the study
Piperine — raw ingredient

Ingredient

Black Pepper (Piperine)

Each bar shows the study’s reported effect, scaled within its own measure — bars are not directly comparable across rows. Every figure is the result of research on the ingredient, not a claim about ProleevaMax.

The studies cited here are research on individual ingredients, not on ProleevaMax. They are presented to explain the science behind the formula and do not constitute a claim that ProleevaMax produces these outcomes.

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

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