Benefits
Skin hydration and elasticity in women aged 40 to 60
In a placebo-controlled trial, 1,000 mg a day of a catfish collagen peptide with over 15 percent tripeptides gave higher skin hydration than placebo at 6 and 12 weeks and better scores on two of three elasticity measures at 12 weeks; 53 of 64 women finished. A second trial of a tilapia tripeptide at the same dose found no difference in hydration, elasticity or its main outcome, skin water loss, unless weather was adjusted for.
Facial wrinkle scores
In the catfish collagen peptide trial, dermatologist wrinkle grades and three of five wrinkle depth measures from skin replicas improved more than with placebo after 12 weeks of 1,000 mg a day. In the tilapia tripeptide trial, wrinkle grades and wrinkle measures did not differ from placebo. Both trials involved employees of the product makers.
Thigh skin smoothness, skin elasticity and hair thickness
In 114 women aged 20 to 50 with thigh cellulite and thinning hair, a fish collagen peptide rich in Gly-Pro-Hyp at 1,000 mg a day for 24 weeks improved cellulite severity, skin roughness and elasticity more than placebo at weeks 12 and 24, and hair diameter at week 24. Two of the five authors worked for Newtree, which makes this type of peptide.
Knee pain and physical function scores
In 80 adults aged 40 to 75 with early knee joint wear, 3,000 mg a day of a peptide with over 15 percent tripeptides for 180 days lowered the main outcome, a WOMAC knee pain score, more than placebo. Function and total scores also improved; a 100 mm pain scale, stiffness, joint space width and inflammation markers did not differ. Only 60 of 80 were analyzed. Funded by the maker, Newtree.
Arterial stiffness, a vascular marker
In an open-label study without a control group, 30 healthy adults took 16 g a day of Jellice collagen tripeptide for 6 months. An arterial stiffness index (CAVI) fell by about 0.2 points, and the LDL to HDL cholesterol ratio fell in those starting at 2.5 or higher. Two authors were Jellice employees. No placebo trial has tested this.
Mechanism of action
Tripeptides reach the blood intact
In a Jellice study in people, plasma Gly-Pro-Hyp and Pro-Hyp rose after collagen tripeptide preparations, and more with more Gly-Pro-Hyp eaten; both also appeared in urine. Other makers report similar higher blood Gly-Pro-Hyp than with ordinary collagen. Blood levels are a marker, not a health result.
Gly-Pro-Hyp as a signal to skin cells in the lab
In rats, Gly-Pro-Hyp and Pro-Hyp from a tripeptide product stayed stable in gut fluid and plasma for 2 hours, and Gly-Pro-Hyp crossed a layer of intestinal cells. In cultured human skin fibroblasts, Gly-Pro-Hyp limited the fall in collagen and elastin gene activity caused by oxidative stress. These are lab and animal findings, not trials in people.
How it differs from ordinary collagen peptides
Ordinary collagen peptides are mostly larger fragments. Tripeptide products are cut further by specific enzymes, such as a Bacillus collagenase for Amicogen's tilapia product, to keep intact Gly-X-Y units. No placebo-controlled trial found compares skin or joint outcomes of a tripeptide product head to head with an ordinary collagen peptide in healthy people.
Clinical trials
Randomized, double-blind, placebo-controlled parallel trial; one 50 mL drink with 1,000 mg of low-molecular-weight collagen peptide (over 15 percent tripeptides including 3 percent Gly-Pro-Hyp, from Newtree) daily for 12 weeks; both drinks contained 100 mg vitamin C; no primary outcome named; per-protocol analysis; two authors from Newtree and one from Jellice; no external funding (Kim et al. 2018, Nutrients)
64 women aged 40 to 60 with crow's feet wrinkles randomized (33 test, 31 placebo); 53 completed.
Skin hydration was higher than placebo at 6 and 12 weeks. At 12 weeks the dermatologist wrinkle grade (p = 0.013) and three wrinkle replica measures (p = 0.043, 0.025 and 0.004) improved more than placebo, as did overall and net skin elasticity (p = 0.025 and 0.027). No adverse reactions were reported and blood and urine tests stayed normal.
Randomized, double-blind, placebo-controlled parallel trial; 1,000 mg a day of Collagen-Tripep20S (Amicogen; 20 percent tripeptides including 3.2 percent Gly-Pro-Hyp) or a maltodextrin and dextrin placebo for 12 weeks; registered NCT03505684 after enrollment began, with skin water loss (TEWL) as the primary outcome and no weather adjustment named; three authors employed by Amicogen (Tak et al. 2020, Front Med (Lausanne))
84 women aged 40 to 60 with raised skin water loss; 74 completed.
Primary outcome: at 12 weeks skin water loss fell more on collagen tripeptide (-0.94 versus -0.33 g/m2/h), but the unadjusted between-group test was not significant (p = 0.168); it was significant after adjustment for temperature, humidity and UV exposure (p = 0.024 to 0.032). The 6 week result did not differ. Hydration, elasticity and wrinkle measures did not differ from placebo.
Randomized, placebo-controlled trial of 1,000 mg a day for 24 weeks, preceded by a preliminary blood study; low-molecular-weight collagen peptide from fish skin gelatin enriched in Gly-X-Y tripeptides; primary outcome not named in the abstract; blinding not described in the abstract; two of five authors from Newtree (Hwang et al. 2026, J Med Food)
114 women aged 20 to 50 with thigh cellulite and self-reported hair thinning.
Cellulite severity, the length of the skin and fat border, skin roughness and skin elasticity improved more than placebo at weeks 12 and 24, and hair diameter increased more at week 24. In the preliminary blood study, exposure to Gly-Pro-Hyp over 2 hours was about 54 times higher than after ordinary collagen.
Randomized, double-blind, placebo-controlled parallel trial; 3,000 mg a day (500 mg tablets) of a catfish skin peptide with over 15 percent tripeptides including at least 3 percent Gly-Pro-Hyp for 180 days; registered KCT0005507; funded by and product made by Newtree, with a Newtree employee as author; per-protocol analysis (Park et al. 2025, Front Nutr)
80 adults aged 40 to 75 with grade I or II knee osteoarthritis and knee pain; 60 analyzed (29 test, 31 placebo).
Primary outcome: WOMAC pain fell more than with placebo (-1.90 versus +0.61, p = 0.006). WOMAC function (p = 0.035) and total scores (p = 0.028) also improved more. The 100 mm pain scale (p = 0.299), stiffness, joint space width on X-ray and inflammation markers did not differ. One test participant left because of an adverse event (hives, judged unrelated); no serious events. The collagen group started with higher pain scores (4.45 versus 3.29) and more grade II knees, only per-protocol results were reported, and a published commentary questioned these points.
Open-label, single-arm study without a control group; 16 g a day of Jellice collagen tripeptide (over 15 percent Gly-X-Y tripeptides) in two doses for 6 months; registered UMIN000018525; supported by a Japanese government small business subsidy; two authors employed by Jellice and one described as having been a Jellice board member (Tomosugi et al. 2017, J Atheroscler Thromb)
32 healthy adults (16 men, 16 women); 30 analyzed.
The cardio-ankle vascular index, an arterial stiffness marker, fell from baseline on both sides (p = 0.048 and 0.047), about 0.2 points. Advanced glycation end products in blood fell, and the LDL to HDL cholesterol ratio fell in people starting at 2.5 or higher. Without a placebo group, these changes cannot be attributed to the product.
Randomized controlled trial with a no-supplement control group and no placebo; collagen peptide 3 g a day, collagen peptide 3 g plus vitamin C 500 mg, or vitamin C 500 mg alone for 12 weeks (Choi et al. 2014, J Cosmet Laser Ther)
32 healthy volunteers in four groups.
Changes in skin hydration and elasticity from baseline were greater in both collagen groups than in the no-supplement group. Adding vitamin C did not increase the effect. With about eight people per group and no placebo, the results are weak.
Human absorption study comparing a tripeptide fraction (CTP-100), a preparation with about 50 percent Gly-X-Y tripeptides (CTP-50) and a collagen peptide without tripeptides; all authors from Jellice (Yamamoto et al. 2016, Biol Pharm Bull)
Healthy volunteers (number not stated in the abstract).
Plasma Gly-Pro-Hyp and Pro-Hyp rose after both tripeptide preparations, more with more Gly-Pro-Hyp eaten, and both peptides appeared in urine. This shows absorption, a marker, and does not test any skin, joint or other health outcome.