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0.1.0 | 0.1.0-pilot | BPC-HUM-001 | record-bpc-hum-001 | BPC-157 | PL 14736 / BPC-157 | not reported | uncertain | rectal enema | enema; excipients not reported | 32 healthy male volunteers; 24 received PL 14736 and 8 placebo | Short-term rectal-enema tolerability in healthy men | Attributed adverse events and reported headache or flatulence | Single administration and seven repeated daily administrations | human-administered-safety-or-pk | Placebo-controlled phase 1 study reported only in meeting abstracts | Placebo enema | 32 | not reported | not-evaluable | The abstracts reported no significant attributed adverse events and no obvious difference in headache or flatulence frequency or severity versus placebo. | Numerical adverse-event counts were not reported. | limited-observation-only | abstract-only | small-short-study | form-unresolved | insufficient-safety-characterization | meeting-abstract-only | not found | Marija Veljaca and collaborators | Historical PL 14736 development program; institution not resolved in accessible abstracts | not reported | not reported | No exact-name BPC-157 patent intersection was verified for recurring author Marija Veljaca in the bounded 2026-08-14 Google Patents screen. | The meeting abstracts were not resolved as OpenAlex works; no reproducible cited-by denominator is reported. | Original abstract text was not publicly located. | The FDA dossier is the accessible source for design, exposure and outcome details. | Form, assay detail, numerical adverse-event counts and complete analysis methods are unresolved. | VELJACA-2002 | VELJACA-2003 | FDA-BPC-2026 | https://www.fda.gov/media/193343/download | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-002 | record-bpc-hum-002 | BPC-157 | PL 14736 / BPC-157 | not reported | uncertain | rectal enema | enema; excipients not reported | 32 healthy male volunteers; 24 received PL 14736 and 8 placebo | Systemic pharmacokinetic characterization after rectal enema | Plasma BPC-157 measured by HPLC-MS/MS | After rectal-enema administration | human-administered-safety-or-pk | Placebo-controlled phase 1 study reported only in meeting abstracts | Placebo enema | 32 | not reported | not-evaluable | Most reported plasma concentrations were undetected or below the assay lower limit of quantification; further assay and time-course details were not available. | No extractable Cmax, Tmax, AUC or half-life. | no | below-quantification | abstract-only | assay-details-missing | form-unresolved | meeting-abstract-only | not found | Marija Veljaca and collaborators | Historical PL 14736 development program; institution not resolved in accessible abstracts | not reported | not reported | No exact-name BPC-157 patent intersection was verified for recurring author Marija Veljaca in the bounded 2026-08-14 Google Patents screen. | The meeting abstracts were not resolved as OpenAlex works; no reproducible cited-by denominator is reported. | Original abstract text was not publicly located. | The FDA dossier is the accessible source for design, exposure and outcome details. | Form, assay detail, numerical adverse-event counts and complete analysis methods are unresolved. | VELJACA-2002 | VELJACA-2003 | FDA-BPC-2026 | https://www.fda.gov/media/193343/download | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-003 | record-bpc-hum-003 | BPC-157 | PL 14736 / BPC-157 | not reported | uncertain | rectal enema | liquid enema; excipients not reported | 53 people with mild-to-moderate ulcerative colitis; inclusion definition unclear | Two-week rectal-enema treatment improves mild-to-moderate ulcerative-colitis activity | Change in incompletely defined Disease Activity Index | Two weeks | human-administered-clinical-outcome | Multicenter randomized double-blind placebo-controlled phase 2 study reported as a meeting abstract | Placebo enema | 53 | 46 | not-evaluable | FDA reports mean changes of -3.2 for PL 14736 and -1.6 for placebo, with an estimated between-group difference of 1.6 and a 95% interval from -4.84 to 1.62. | Between-group interval includes no difference; analysis definition and sign convention are insufficiently documented. | no | abstract-only | endpoint-definition-incomplete | interval-includes-null | form-unresolved | enema-does-not-transfer-to-other-routes | meeting-abstract-only | not found | M Ruenzi | M Stolte | Marija Veljaca | K Oreskovic | J Peterson | UCS Group | Historical PL 14736 development program; participating centers not resolved | not reported | not reported | No exact-name BPC-157 patent intersection was verified for recurring author Marija Veljaca in the bounded screen. | The meeting abstract was not resolved as an OpenAlex work; no reproducible cited-by denominator is reported. | Only a meeting abstract was located and the accessible extraction is in the FDA dossier. | Primary endpoint definition, eligibility, statistical methods and post-treatment follow-up are incomplete. | The FDA-reported between-group interval includes no difference and the sign convention is not sufficiently documented fo... | RUENZI-2005 | FDA-BPC-2026 | https://www.fda.gov/media/193343/download | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-004 | record-bpc-hum-004 | BPC-157 | PL 14736 / BPC-157 | not reported | uncertain | rectal enema | liquid enema; excipients not reported | 53 people with mild-to-moderate ulcerative colitis; inclusion definition unclear | Two-week rectal-enema safety in ulcerative colitis | Adverse-event frequency and adverse-event withdrawals | Two weeks | human-administered-safety-or-pk | Multicenter randomized double-blind placebo-controlled phase 2 study reported as a meeting abstract | Placebo enema | 53 | 46 | not-evaluable | The abstract reported similar adverse-event types and frequency; three PL 14736 and two placebo participants withdrew after adverse events described mainly as disease progression. | No complete event table or exposure-adjusted estimate. | limited-observation-only | abstract-only | small-short-study | incomplete-safety-monitoring | form-unresolved | meeting-abstract-only | not found | M Ruenzi | M Stolte | Marija Veljaca | K Oreskovic | J Peterson | UCS Group | Historical PL 14736 development program; participating centers not resolved | not reported | not reported | No exact-name BPC-157 patent intersection was verified for recurring author Marija Veljaca in the bounded screen. | The meeting abstract was not resolved as an OpenAlex work; no reproducible cited-by denominator is reported. | Only a meeting abstract was located and the accessible extraction is in the FDA dossier. | Primary endpoint definition, eligibility, statistical methods and post-treatment follow-up are incomplete. | The FDA-reported between-group interval includes no difference and the sign convention is not sufficiently documented fo... | RUENZI-2005 | FDA-BPC-2026 | https://www.fda.gov/media/193343/download | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-005 | record-bpc-hum-005 | BPC-157 | BPC 157 | not reported | uncertain | intra-articular knee injection | Compounded solution in sodium-phosphate buffer with benzyl alcohol | 17 clinic patients with heterogeneous knee-pain diagnoses; 16 contacted, including 12 BPC-157-only recipients | Intra-articular BPC-157 is followed by self-reported knee-pain improvement | Participant-reported significant knee-pain improvement | Telephone follow-up, usually six to twelve months after injection | human-administered-clinical-outcome | Single-clinic retrospective chart review with later telephone survey | null | not applicable | 16 | supports | Eleven of twelve contacted BPC-157-only recipients reported significant improvement; the study had no control group or validated prespecified pain instrument. | 11/12 BPC-157-only recipients reported improvement. | yes-for-observed-self-report-only | uncontrolled | retrospective | self-reported | heterogeneous-diagnoses | form-unresolved | no-structural-healing-outcome | peer-reviewed-article | not found | Edwin Lee | Blake Padgett | Institute for Hormonal Balance, Orlando, Florida | University of Central Florida College of Medicine | not reported | Authors did not provide a conflict statement in the accessible paper; patients paid for product and procedure. | No exact-name BPC-157 patent intersection was verified for Edwin Lee in the bounded screen. | OpenAlex reported 15 citing works on 2026-08-14; this is metadata coverage, not a quality measure. | No randomization, control group, blinded assessment or prespecified validated outcome instrument. | Diagnoses and follow-up were heterogeneous; one participant was unreachable. | Four participants received BPC-157 with thymosin beta-4 and are not used for the BPC-157-only claim record. | No post-treatment imaging estab... | LEE-PADGETT-2021 | FDA-BPC-2026 | OPENALEX-2026-08-14 | GOOGLE-PATENTS-2026-08-14 | https://pubmed.ncbi.nlm.nih.gov/34324435/ | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-006 | record-bpc-hum-006 | BPC-157 | BPC 157 | not reported | uncertain | intra-articular knee injection | Compounded solution in sodium-phosphate buffer with benzyl alcohol | 17 clinic patients with heterogeneous knee-pain diagnoses; 16 contacted, including 12 BPC-157-only recipients | Intra-articular BPC-157 is safe | Participant-reported adverse events | Retrospective telephone follow-up | human-administered-safety-or-pk | Single-clinic retrospective chart review with later telephone survey | null | not applicable | 16 | not-evaluable | The paper states that no adverse events were noted, but safety monitoring was retrospective, unstructured and too small to characterize safety. | No coded adverse-event table. | limited-observation-only | uncontrolled | retrospective | small-sample | informal-safety-ascertainment | form-unresolved | peer-reviewed-article | not found | Edwin Lee | Blake Padgett | Institute for Hormonal Balance, Orlando, Florida | University of Central Florida College of Medicine | not reported | Authors did not provide a conflict statement in the accessible paper; patients paid for product and procedure. | No exact-name BPC-157 patent intersection was verified for Edwin Lee in the bounded screen. | OpenAlex reported 15 citing works on 2026-08-14; this is metadata coverage, not a quality measure. | No randomization, control group, blinded assessment or prespecified validated outcome instrument. | Diagnoses and follow-up were heterogeneous; one participant was unreachable. | Four participants received BPC-157 with thymosin beta-4 and are not used for the BPC-157-only claim record. | No post-treatment imaging estab... | LEE-PADGETT-2021 | FDA-BPC-2026 | OPENALEX-2026-08-14 | GOOGLE-PATENTS-2026-08-14 | https://pubmed.ncbi.nlm.nih.gov/34324435/ | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-007 | record-bpc-hum-007 | BPC-157 | BPC-157 | not reported | uncertain | intravesical injections into bladder uroepithelium | Compounded injectable solution; excipients not reported | 12 women aged 39-76 with moderate-to-severe interstitial cystitis and prior pentosan-polysulfate nonresponse | One intravesical BPC-157 procedure is followed by improved interstitial-cystitis symptoms | Global Response Assessment and participant-reported symptom resolution | Six-week clinical follow-up; most questionnaires at four to six months | human-administered-clinical-outcome | Single-clinic uncontrolled retrospective pilot with Global Response Assessment | null | not applicable | 12 | supports | All 12 participants scored 5/5 on the Global Response Assessment; ten reported complete resolution and two reported 80% improvement. | 12/12 rated significantly improved in an uncontrolled selected sample. | yes-for-observed-self-report-only | uncontrolled | retrospective | self-reported | selected-private-clinic-sample | variable-follow-up | form-unresolved | peer-reviewed-article | not found | Edwin Lee | Christopher Walker | Bahram Ayadi | UroGyn Specialists of Florida | University of Central Florida College of Medicine | No funding statement located in the paper | Authors declared no conflict; all participants paid for BPC-157 and received no honorarium. | No exact-name BPC-157 patent intersection was verified for Edwin Lee in the bounded screen. | OpenAlex reported 5 citing works on 2026-08-14; this is metadata coverage, not a quality measure. | No sham control, blinding or prespecified statistical comparison. | Small selected private-clinic sample with self-reported outcome and variable questionnaire timing. | Product identity and form were not independently verified. | The paper's causal and safety conclusions exceed what the design can establish. | LEE-WALKER-AYADI-2024 | FDA-BPC-2026 | OPENALEX-2026-08-14 | GOOGLE-PATENTS-2026-08-14 | https://pubmed.ncbi.nlm.nih.gov/39325560/ | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-008 | record-bpc-hum-008 | BPC-157 | BPC-157 | not reported | uncertain | intravesical injections into bladder uroepithelium | Compounded injectable solution; excipients not reported | 12 women aged 39-76 with moderate-to-severe interstitial cystitis and prior pentosan-polysulfate nonresponse | One intravesical BPC-157 procedure is safe | Dropout, reported symptoms and post-procedural complications | Through reported follow-up | human-administered-safety-or-pk | Single-clinic uncontrolled retrospective pilot with Global Response Assessment | null | not applicable | 12 | not-evaluable | No participant dropped out and the paper reports no adverse events or listed post-procedural complications, but the sample and design cannot characterize safety. | 0/12 reported events in the paper's limited ascertainment. | limited-observation-only | uncontrolled | small-sample | informal-safety-ascertainment | form-unresolved | peer-reviewed-article | not found | Edwin Lee | Christopher Walker | Bahram Ayadi | UroGyn Specialists of Florida | University of Central Florida College of Medicine | No funding statement located in the paper | Authors declared no conflict; all participants paid for BPC-157 and received no honorarium. | No exact-name BPC-157 patent intersection was verified for Edwin Lee in the bounded screen. | OpenAlex reported 5 citing works on 2026-08-14; this is metadata coverage, not a quality measure. | No sham control, blinding or prespecified statistical comparison. | Small selected private-clinic sample with self-reported outcome and variable questionnaire timing. | Product identity and form were not independently verified. | The paper's causal and safety conclusions exceed what the design can establish. | LEE-WALKER-AYADI-2024 | FDA-BPC-2026 | OPENALEX-2026-08-14 | GOOGLE-PATENTS-2026-08-14 | https://pubmed.ncbi.nlm.nih.gov/39325560/ | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-009 | record-bpc-hum-009 | BPC-157 | BPC-157 | not reported | uncertain | intravenous infusion | Compounded BPC-157 diluted in normal saline | Two relatively healthy adults aged 58 and 68, both previously exposed to intravenous BPC-157 | Two consecutive intravenous BPC-157 infusions are safe | Solicited immediate adverse events | During infusions through 24 hours after the second infusion | human-administered-safety-or-pk | Single-center uncontrolled short-term pilot | Within-person baseline only | not applicable | 2 | not-evaluable | Neither of two previously exposed participants reported the solicited adverse reactions during the very short observation window. | 0/2 reported solicited events. | limited-observation-only | two-participants | previously-exposed | no-control | very-short-follow-up | form-unresolved | peer-reviewed-article | not found | Edwin Lee | Kailynd Burgess | Institute for Hormonal Balance, Orlando, Florida | Access Medical Labs | The paper states that the research received no funding | Authors declared no conflict; both participants paid $1,000 for product and laboratory work and volunteered to support continued compounding. | No exact-name BPC-157 patent intersection was verified for Edwin Lee in the bounded screen. | OpenAlex reported 3 citing works on 2026-08-14; this is metadata coverage, not a quality measure. | Two previously exposed participants cannot characterize uncommon, delayed or first-exposure harms. | No placebo, blinding, formal adverse-event coding or follow-up beyond the next day. | The observed laboratory range cannot establish general safety. | LEE-BURGESS-2025 | FDA-BPC-2026 | OPENALEX-2026-08-14 | GOOGLE-PATENTS-2026-08-14 | https://pubmed.ncbi.nlm.nih.gov/40131143/ | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-HUM-010 | record-bpc-hum-010 | BPC-157 | BPC-157 | not reported | uncertain | intravenous infusion | Compounded BPC-157 diluted in normal saline | Two relatively healthy adults aged 58 and 68, both previously exposed to intravenous BPC-157 | Two consecutive intravenous BPC-157 infusions cause no clinically meaningful short-term laboratory or vital-sign change | Selected vital signs, metabolic, blood-count, cardiac, thyroid and inflammation biomarkers | Baseline through 24 hours after the second infusion | human-administered-pd-or-biomarker | Single-center uncontrolled short-term pilot | Within-person baseline only | not applicable | 2 | null | The authors reported no clinically meaningful change in the selected measures across the two participants and three measurement days. | Individual values only; no inferential estimate. | yes-for-observed-window-only | two-participants | no-control | multiple-selected-biomarkers | very-short-follow-up | cannot-establish-general-safety | peer-reviewed-article | not found | Edwin Lee | Kailynd Burgess | Institute for Hormonal Balance, Orlando, Florida | Access Medical Labs | The paper states that the research received no funding | Authors declared no conflict; both participants paid $1,000 for product and laboratory work and volunteered to support continued compounding. | No exact-name BPC-157 patent intersection was verified for Edwin Lee in the bounded screen. | OpenAlex reported 3 citing works on 2026-08-14; this is metadata coverage, not a quality measure. | Two previously exposed participants cannot characterize uncommon, delayed or first-exposure harms. | No placebo, blinding, formal adverse-event coding or follow-up beyond the next day. | The observed laboratory range cannot establish general safety. | LEE-BURGESS-2025 | FDA-BPC-2026 | OPENALEX-2026-08-14 | GOOGLE-PATENTS-2026-08-14 | https://pubmed.ncbi.nlm.nih.gov/40131143/ | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-001 | record-bpc-reg-001 | BPC-157 | Bepecin / PCO-02 / BPC-157 | not reported | uncertain | oral tablet | PCO-02 tablet | Estimated 42 healthy volunteers in Tijuana, Mexico | Oral PCO-02 safety in healthy volunteers | Any adverse event | Six months | registered-only | Randomized quadruple-masked placebo-controlled phase 1 registry record | PCO-03 placebo tablets | 42 | not reported | not-evaluable | The registry planned this outcome but has stale status and no posted results or matched publication. | No result available. | no-result | registry-only | status-unknown | no-results | form-unresolved | no-results-publication-located | unknown; last known active, not recruiting; record not updated since 2015-12-22 | Rufino Menchaca (registry principal investigator) | PharmaCotherapia d.o.o. | Hospital Angeles Tijuana | Industry lead sponsor: PharmaCotherapia d.o.o. | not reported | No investigator-level patent match was established in this pilot. | Not applicable until a results work is matched. | Registry status is stale and no results are posted. | A 2016 results submission was later unreleased for an unknown reason according to registry history metadata. | No peer-reviewed publication was matched by identifier or study characteristics. | NCT02637284 | FDA-BPC-2026 | https://clinicaltrials.gov/study/NCT02637284 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-002 | record-bpc-reg-002 | BPC-157 | Bepecin / PCO-02 / BPC-157 | not reported | uncertain | oral tablet | PCO-02 tablet | Estimated 42 healthy volunteers in Tijuana, Mexico | Oral PCO-02 pharmacokinetics in healthy volunteers | Cmax, Tmax, AUC and elimination half-life | 168 hours | registered-only | Randomized quadruple-masked placebo-controlled phase 1 registry record | PCO-03 placebo tablets | 42 | not reported | not-evaluable | The registry planned pharmacokinetic outcomes but has no posted values or matched publication. | No result available. | no-result | registry-only | status-unknown | no-results | form-unresolved | no-results-publication-located | unknown; last known active, not recruiting; record not updated since 2015-12-22 | Rufino Menchaca (registry principal investigator) | PharmaCotherapia d.o.o. | Hospital Angeles Tijuana | Industry lead sponsor: PharmaCotherapia d.o.o. | not reported | No investigator-level patent match was established in this pilot. | Not applicable until a results work is matched. | Registry status is stale and no results are posted. | A 2016 results submission was later unreleased for an unknown reason according to registry history metadata. | No peer-reviewed publication was matched by identifier or study characteristics. | NCT02637284 | FDA-BPC-2026 | https://clinicaltrials.gov/study/NCT02637284 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-003 | record-bpc-reg-003 | BPC-157 | Pentadecapeptide BPC 157 | not reported | uncertain | subcutaneous injection | Identical-appearing prefilled syringe; composition not reported | Planned 120 participants with acute MRI-confirmed grade II hamstring strain in Shenzhen, China | Subcutaneous BPC-157 accelerates return to unrestricted sport after acute grade II hamstring strain | Days to clinician-cleared unrestricted sport plus functional battery | Eight weeks | registered-only | Randomized quadruple-masked placebo-controlled phase 2 trial with standardized rehabilitation | Matching placebo plus the same rehabilitation program | 120 | not yet available | not-evaluable | The randomized trial is recruiting and has no posted results. | No result available. | no-result | registry-only | recruiting | no-results | dose-and-form-unresolved | no-results-publication-located | recruiting; no results posted | Hudson Biotech registry team; individual investigator not listed | Hudson Biotech | Peking University Shenzhen Hospital | Industry lead sponsor: Hudson Biotech | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | Registry-only planned outcomes cannot establish efficacy or safety. | Dose, form and product identity are not reported. | The registry maps both active and placebo intervention names to both arms, creating an internal arm-label ambiguity. | NCT07437547 | https://clinicaltrials.gov/study/NCT07437547 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-004 | record-bpc-reg-004 | BPC-157 | Pentadecapeptide BPC 157 | not reported | uncertain | subcutaneous injection | Identical-appearing prefilled syringe; composition not reported | Planned 120 participants with acute MRI-confirmed grade II hamstring strain in Shenzhen, China | Subcutaneous BPC-157 reduces MRI-assessed hamstring injury volume | Change in centrally reviewed MRI injury volume | Day 14 | registered-only | Randomized quadruple-masked placebo-controlled phase 2 trial with standardized rehabilitation | Matching placebo plus the same rehabilitation program | 120 | not yet available | not-evaluable | The randomized trial is recruiting and has no posted results. | No result available. | no-result | registry-only | recruiting | no-results | dose-and-form-unresolved | no-results-publication-located | recruiting; no results posted | Hudson Biotech registry team; individual investigator not listed | Hudson Biotech | Peking University Shenzhen Hospital | Industry lead sponsor: Hudson Biotech | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | Registry-only planned outcomes cannot establish efficacy or safety. | Dose, form and product identity are not reported. | The registry maps both active and placebo intervention names to both arms, creating an internal arm-label ambiguity. | NCT07437547 | https://clinicaltrials.gov/study/NCT07437547 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-005 | record-bpc-reg-005 | BPC-157 | Parlay Recover gummies containing Body Protection Compound (BPC)-157 | not reported | uncertain | oral gummy | Commercial peptide gummy | 40 physically active US adults aged 18-65 with recurrent post-exercise musculoskeletal symptoms | BPC-157-labeled gummies change systemic inflammation | Change in high-sensitivity C-reactive protein | Baseline to week 8 | registered-only | Single-group open-label industry study registered after study completion | null | not applicable | not reported | not-evaluable | The completed, retrospectively registered single-group study has no posted results. | No result available. | no-result | registry-only | retrospective-registration | no-control | no-results | finished-product-identity-unresolved | no-results-publication-located | completed 2025-11-01; first submitted 2026-08-03; no results posted | Parlay Wellness registry team; individual investigator not listed | Parlay Wellness | Citruslabs | Industry lead sponsor: Parlay Wellness; industry collaborator: Citruslabs | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | The registry was first submitted about nine months after reported study completion. | No comparator, blinding, posted results or matched publication. | Finished-product identity and the contribution of BPC-157 versus other product attributes are unresolved. | NCT07752381 | https://clinicaltrials.gov/study/NCT07752381 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-006 | record-bpc-reg-006 | BPC-157 | Parlay Recover gummies containing Body Protection Compound (BPC)-157 | not reported | uncertain | oral gummy | Commercial peptide gummy | 40 physically active US adults aged 18-65 with recurrent post-exercise musculoskeletal symptoms | BPC-157-labeled gummies change systemic inflammation | Change in interleukin-6 | Baseline to week 8 | registered-only | Single-group open-label industry study registered after study completion | null | not applicable | not reported | not-evaluable | The completed, retrospectively registered single-group study has no posted results. | No result available. | no-result | registry-only | retrospective-registration | no-control | no-results | finished-product-identity-unresolved | no-results-publication-located | completed 2025-11-01; first submitted 2026-08-03; no results posted | Parlay Wellness registry team; individual investigator not listed | Parlay Wellness | Citruslabs | Industry lead sponsor: Parlay Wellness; industry collaborator: Citruslabs | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | The registry was first submitted about nine months after reported study completion. | No comparator, blinding, posted results or matched publication. | Finished-product identity and the contribution of BPC-157 versus other product attributes are unresolved. | NCT07752381 | https://clinicaltrials.gov/study/NCT07752381 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-007 | record-bpc-reg-007 | BPC-157 | Parlay Recover gummies containing Body Protection Compound (BPC)-157 | not reported | uncertain | oral gummy | Commercial peptide gummy | 40 physically active US adults aged 18-65 with recurrent post-exercise musculoskeletal symptoms | BPC-157-labeled gummies reduce perceived muscle or joint swelling | Change in self-reported swelling | Baseline through week 8 | registered-only | Single-group open-label industry study registered after study completion | null | not applicable | not reported | not-evaluable | The completed, retrospectively registered single-group study has no posted results. | No result available. | no-result | registry-only | retrospective-registration | no-control | self-reported | no-results | finished-product-identity-unresolved | no-results-publication-located | completed 2025-11-01; first submitted 2026-08-03; no results posted | Parlay Wellness registry team; individual investigator not listed | Parlay Wellness | Citruslabs | Industry lead sponsor: Parlay Wellness; industry collaborator: Citruslabs | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | The registry was first submitted about nine months after reported study completion. | No comparator, blinding, posted results or matched publication. | Finished-product identity and the contribution of BPC-157 versus other product attributes are unresolved. | NCT07752381 | https://clinicaltrials.gov/study/NCT07752381 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-008 | record-bpc-reg-008 | BPC-157 | Parlay Recover gummies containing Body Protection Compound (BPC)-157 | not reported | uncertain | oral gummy | Commercial peptide gummy | 40 physically active US adults aged 18-65 with recurrent post-exercise musculoskeletal symptoms | BPC-157-labeled gummies reduce post-exercise aching | Change in self-reported aching | Baseline through week 8 | registered-only | Single-group open-label industry study registered after study completion | null | not applicable | not reported | not-evaluable | The completed, retrospectively registered single-group study has no posted results. | No result available. | no-result | registry-only | retrospective-registration | no-control | self-reported | no-results | finished-product-identity-unresolved | no-results-publication-located | completed 2025-11-01; first submitted 2026-08-03; no results posted | Parlay Wellness registry team; individual investigator not listed | Parlay Wellness | Citruslabs | Industry lead sponsor: Parlay Wellness; industry collaborator: Citruslabs | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | The registry was first submitted about nine months after reported study completion. | No comparator, blinding, posted results or matched publication. | Finished-product identity and the contribution of BPC-157 versus other product attributes are unresolved. | NCT07752381 | https://clinicaltrials.gov/study/NCT07752381 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-009 | record-bpc-reg-009 | BPC-157 | Parlay Recover gummies containing Body Protection Compound (BPC)-157 | not reported | uncertain | oral gummy | Commercial peptide gummy | 40 physically active US adults aged 18-65 with recurrent post-exercise musculoskeletal symptoms | BPC-157-labeled gummies reduce post-exercise stiffness | Change in self-reported stiffness | Baseline through week 8 | registered-only | Single-group open-label industry study registered after study completion | null | not applicable | not reported | not-evaluable | The completed, retrospectively registered single-group study has no posted results. | No result available. | no-result | registry-only | retrospective-registration | no-control | self-reported | no-results | finished-product-identity-unresolved | no-results-publication-located | completed 2025-11-01; first submitted 2026-08-03; no results posted | Parlay Wellness registry team; individual investigator not listed | Parlay Wellness | Citruslabs | Industry lead sponsor: Parlay Wellness; industry collaborator: Citruslabs | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | The registry was first submitted about nine months after reported study completion. | No comparator, blinding, posted results or matched publication. | Finished-product identity and the contribution of BPC-157 versus other product attributes are unresolved. | NCT07752381 | https://clinicaltrials.gov/study/NCT07752381 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-010 | record-bpc-reg-010 | BPC-157 | Parlay Recover gummies containing Body Protection Compound (BPC)-157 | not reported | uncertain | oral gummy | Commercial peptide gummy | 40 physically active US adults aged 18-65 with recurrent post-exercise musculoskeletal symptoms | BPC-157-labeled gummies improve perceived muscle function | Change in self-reported muscle function | Baseline through week 8 | registered-only | Single-group open-label industry study registered after study completion | null | not applicable | not reported | not-evaluable | The completed, retrospectively registered single-group study has no posted results. | No result available. | no-result | registry-only | retrospective-registration | no-control | self-reported | no-results | finished-product-identity-unresolved | no-results-publication-located | completed 2025-11-01; first submitted 2026-08-03; no results posted | Parlay Wellness registry team; individual investigator not listed | Parlay Wellness | Citruslabs | Industry lead sponsor: Parlay Wellness; industry collaborator: Citruslabs | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | The registry was first submitted about nine months after reported study completion. | No comparator, blinding, posted results or matched publication. | Finished-product identity and the contribution of BPC-157 versus other product attributes are unresolved. | NCT07752381 | https://clinicaltrials.gov/study/NCT07752381 | [object Object] |
0.1.0 | 0.1.0-pilot | BPC-REG-011 | record-bpc-reg-011 | BPC-157 | Parlay Recover gummies containing Body Protection Compound (BPC)-157 | not reported | uncertain | oral gummy | Commercial peptide gummy | 40 physically active US adults aged 18-65 with recurrent post-exercise musculoskeletal symptoms | BPC-157-labeled gummies improve perceived exercise recovery | Change in self-reported muscle and joint recovery | Baseline through week 8 | registered-only | Single-group open-label industry study registered after study completion | null | not applicable | not reported | not-evaluable | The completed, retrospectively registered single-group study has no posted results. | No result available. | no-result | registry-only | retrospective-registration | no-control | self-reported | no-results | finished-product-identity-unresolved | no-results-publication-located | completed 2025-11-01; first submitted 2026-08-03; no results posted | Parlay Wellness registry team; individual investigator not listed | Parlay Wellness | Citruslabs | Industry lead sponsor: Parlay Wellness; industry collaborator: Citruslabs | not reported | No sponsor or investigator patent match was established in this pilot. | Not applicable until a results work is matched. | The registry was first submitted about nine months after reported study completion. | No comparator, blinding, posted results or matched publication. | Finished-product identity and the contribution of BPC-157 versus other product attributes are unresolved. | NCT07752381 | https://clinicaltrials.gov/study/NCT07752381 | [object Object] |
Seven FDA-reviewed peptides: claims coded for identity, administration, outcome and replication
A claim-level comparison of the seven peptide pairs reviewed at the FDA Pharmacy Compounding Advisory Committee meeting of 23-24 July 2026. The data separates molecular identity, administration to people, claimed outcomes and independent replication.
Read the evidence-led article: https://lifesco.re/edge/which-peptide-claims-have-actually-been-tested-in-people/
Archived version and DOI: https://doi.org/10.5281/zenodo.22018753
What the coding shows
- Four of the seven peptides have a located administered-human record.
- One has a registered trial with no posted results at the review date.
- None clears all four transfer gates; independent replication is a stop for all seven.
Scope and responsible use
This is editorial evidence synthesis, not medical or treatment guidance, a molecule score, or proof that an untested claim is false.
The complete selection rules, gate definitions, limitations, independence
statement and versioning policy travel with the data in PROTOCOL.md. The
CSV files are intended for tabular exploration; the JSON files preserve the
full structured record and source notes.
Provenance
- Publisher: lifescore Edge
- Editorial methodology and correction route: https://lifesco.re/edge/methodology/
- Dataset version: 1.0.0
- Evidence reviewed: 2026-08-15
- Licence: CC BY 4.0, limited to the original selection, scheme, coding and text described in
PROTOCOL.md
Citation
@dataset{lifescore_fda_peptide_human_evidence_1_0_0,
author = {{lifescore}},
title = {Seven FDA-reviewed peptides: claims coded for identity, administration, outcome and replication},
year = {2026},
version = {1.0.0},
publisher = {lifescore},
doi = {10.5281/zenodo.22018753},
url = {https://doi.org/10.5281/zenodo.22018753}
}
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