U.S. label record. The cited DailyMed label identifies Setmelanotide and contains the product's official indications and warnings. This profile links to the label without restating it as medical guidance.↗
A bounded review of sponsor-funded Phase 3 studies in rare genetic obesity syndromes: two small single-arm trials with withdrawal periods and one randomized trial followed by an open-label period.↗↗
What the reviewed sources report
The reviewed studies reported substantial weight reductions in some participants with specific genetic diagnoses. The cohorts were very small, and the Bardet-Biedl and Alström trial reported inconclusive results for the Alström subgroup.↗↗
What remains unresolved?
How durable are benefits and harms across each genetic subgroup, and which baseline features predict response in these exceptionally small populations?↗↗
The label covers acquired hypothalamic obesity from age four, and Bardet-Biedl syndrome or specified genetically confirmed POMC, PCSK1 or LEPR deficiency from age two. It explicitly excludes general polygenic obesity and specified benign genetic variants. Label: 1 ↗
Which safety limits matter?
Warnings address sexual-arousal effects, depression or suicidal ideation, serious hypersensitivity, pigmentary changes and new or darkened nevi. For acquired hypothalamic obesity, the label adds acute adrenal insufficiency and, with central diabetes insipidus, sodium imbalance. Label: 4, 5 ↗
Label edition and source pins
U.S. product labeling hosted by the National Library of Medicine. This account concerns this product and label edition; other formulations and jurisdictions require their own records.
Label ZIP SHA-256: 3a9024abc434e828923d30e4f860e834f3887ceece2a7a47cdc1c8828105e6f1. Extracted XML SHA-256: b144f343fa74b6d436776a8f7fcb548db348e1c7ffcc8e567930b96cd3b1b812.
Reviews summarize selected studies; their scope and limitations are shown above.
European medicine records · 1 products or applications
EMA medicine metadata checked 2026-09-15. These are product-specific centralized records; national European authorizations and full product-information assessments require separate coverage.
Active substance as listed: setmelanotide. EMA record ↗
Marketing authorisation: 2021-07-16. EMA metadata last updated 2026-05-27. EMA metadata ↗
Application withdrawal and refusal are distinct from marketing authorization. A withdrawal status alone does not establish why it occurred. These metadata entries do not substitute for indication, population or safety details in the relevant product information.
Search and screening record checked 2026-09-15. Counts describe records, not independent trials. Full-text appraisal is separate from an abstract review.
Catalog-name and calibrated alias discovery for human evidence review. Complete query retrieval is separate from clinical eligibility, study-family linkage and appraisal.
219 retrieved · 2 included · 0 excluded · 217 awaiting a decision · 0 full-text appraisals
Search terms, record decisions and remaining work
"Setmelanotide"[Title/Abstract] OR "RM-493"[Title/Abstract] OR "Imcivree"[Title/Abstract]
Retrieved IDs completely represent this query response, not all relevant literature. Additional aliases, references and non-PubMed sources require separate searches.
Unscreened records may include animal or cell experiments, reviews, secondary analyses, mixtures, protocols and unrelated name matches.
Study-family mappings use available declared registry IDs; unresolved mappings do not create independent trial counts. Full-text, corrections and registry comparison remain separate work.
Linked correction notices require comparison with the selected reports: PMID36702567 for PMID36356613. Their presence does not establish what changed.
Showing 25 of 219 record decisions, with included studies and unresolved records first. The versioned data inventory retains every record and study-family link.
PubMed 36356613 — include: Selected published human report; abstract reviewed. Full-text and study-family appraisal remain separate. Study families: NCT03746522.Bibliographic record recheck · 2026-09-15
The selected PubMed XML payload matches the previous reviewed snapshot. This is a metadata recheck, not a new appraisal or a finding that no corrections exist. Open PubMed record ↗
Notice XML SHA-256 a0364c9a387205af00c7ef59f2a4f630522dad75053e75334a3e71fe49db4b0d.
PubMed 33137293 — include: Selected published human report; abstract reviewed. Full-text and study-family appraisal remain separate. Study families: NCT02896192; NCT03287960.Bibliographic record recheck · 2026-09-15
The selected PubMed XML payload matches the previous reviewed snapshot. This is a metadata recheck, not a new appraisal or a finding that no corrections exist. Open PubMed record ↗
PubMed 42737637 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42697206 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42626294 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42611594 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42672527 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42592034 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42538728 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42528856 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42499770 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42498078 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42496807 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42479131 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42466340 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42418774 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42340853 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42339090 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42329358 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42325616 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42475468 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42259622 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42209772 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42205046 — not screened: Name-query match awaiting clinical eligibility screening.
PubMed 42114845 — not screened: Name-query match awaiting clinical eligibility screening.
FDA search
Active-ingredient name query in openFDA Drugs@FDA. Returned application identities include salt forms and combination products; exact indications, approval conditions, supplements and marketing status require document-level review.
1 retrieved · 1 included · 0 excluded · 0 awaiting a decision · 0 full-text appraisals
Zero results describe this query response only, not absence of FDA approval or worldwide nonapproval.
This endpoint does not inventory every label, advisory proceeding, safety communication or regulatory document. Application inclusion does not establish current marketing or approval of every use.
Showing 1 of 1 record decisions, with included studies and unresolved records first. The versioned data inventory retains every record and study-family link.
FDA NDA213793 — include: Retrieved application lists a matching ingredient or its salt; document and product review remain separate. Listed ingredients: SETMELANOTIDE ACETATE.
EMA search
Local matching in the pinned EMA medicines feed; document matches also use identified EMA product numbers. This is not every national European record.
1 retrieved · 1 included · 0 excluded · 0 awaiting a decision · 0 full-text appraisals
Document appraisal and national European sources remain open.
Zero matches apply only to these feed fields and terms; orphan designation is not approval.
Showing 1 of 1 record decisions, with included studies and unresolved records first. The versioned data inventory retains every record and study-family link.
EMA EMEA/H/C/005089 — include: EMA feed product Imcivree; reported status: Authorised. Exact indication and decision documents remain unappraised.
EMA search
Local matching in the pinned EMA documents feed; document matches also use identified EMA product numbers. This is not every national European record.
32 retrieved · 14 included · 0 excluded · 18 awaiting a decision · 0 full-text appraisals
Document appraisal and national European sources remain open.
Zero matches apply only to these feed fields and terms; orphan designation is not approval.
Showing 25 of 32 record decisions, with included studies and unresolved records first. The versioned data inventory retains every record and study-family link.
EMA 52006 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - All authorised presentations
EMA 52007 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - Public assessment report
EMA 52010 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - Orphan maintenance assessment report (initial authorisation)
EMA 56230 — include: Document linked by EMA product number; content unappraised. Imcivree-H-C-005089-II-0002-G : EPAR - Assessment report - Variation
EMA 56231 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - Orphan maintenance assessment report (post authorisation)
EMA 64908 — include: Document linked by EMA product number; content unappraised. Imcivree-H-C-005089-P46-009 : EPAR - Assessment report
EMA 52988 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - Procedural steps taken and scientific information after authorisation (archive)
EMA 52008 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - Risk management plan
EMA 73856 — include: Document linked by EMA product number; content unappraised. Imcivree-VR-0000288021 : EPAR - Assessment report - Variation
EMA 73857 — include: Document linked by EMA product number; content unappraised. Imcivree : Orphan maintenance assessment report (post authorisation)
EMA 52004 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - Medicine overview
EMA 72292 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - Procedural steps taken and scientific information after authorisation
EMA 52005 — include: Document linked by EMA product number; content unappraised. Imcivree : EPAR - Product information
EMA 65061 — include: Document linked by EMA product number; content unappraised. Imcivree-H-C-005089-II-0018 : EPAR - Assessment report - Variation
EMA 14179 — not screened: Title-name match awaiting identity and document review. EU/3/16/1703: Public summary of opinion on orphan designation: Setmelanotide for the treatment of pro-opiomelanocortin deficiency
EMA 31788 — not screened: Title-name match awaiting identity and document review. EU/3/16/1688: Public summary of opinion on orphan designation: Setmelanotide for the treatment of Prader-Willi syndrome
EMA 43893 — not screened: Title-name match awaiting identity and document review. EU/3/18/2101: Public summary of opinion on orphan designation: Setmelanotide for the treatment of leptin receptor deficiency
EMA 46421 — not screened: Title-name match awaiting identity and document review. EU/3/05/269: Public summary of positive opinion for orphan designation of setmelanotide for the treatment of Bardet Biedl syndrome
EMA 47738 — not screened: Title-name match awaiting identity and document review. EU/3/19/2245: Public summary of opinion on orphan designation for setmelanotide for the treatment of Alström syndrome
EMA 51223 — not screened: Title-name match awaiting identity and document review. CHMP summary of positive opinion for Imcivree
EMA 55624 — not screened: Title-name match awaiting identity and document review. Questions and answers on the withdrawal of application to change the marketing authorisation for Imcivree (setmelanotide)
EMA 55626 — not screened: Title-name match awaiting identity and document review. Withdrawal letter: Imcivree
EMA 55632 — not screened: Title-name match awaiting identity and document review. CHMP post-authorisation summary of positive opinion for Imcivree (II-02-G)
EMA 56223 — not screened: Title-name match awaiting identity and document review. Withdrawal assessment report for Imcivree
EMA 63789 — not screened: Title-name match awaiting identity and document review. CHMP post-authorisation summary of positive opinion for Imcivree (II-18)
EMA search
Local matching in the pinned EMA orphans feed; document matches also use identified EMA product numbers. This is not every national European record.
6 retrieved · 6 included · 0 excluded · 0 awaiting a decision · 0 full-text appraisals
Document appraisal and national European sources remain open.
Zero matches apply only to these feed fields and terms; orphan designation is not approval.
Showing 6 of 6 record decisions, with included studies and unresolved records first. The versioned data inventory retains every record and study-family link.
EMA EU/3/23/2833 — include: EMA orphan feed identifies setmelanotide; designation status: Positive. Orphan designation is not marketing authorization.
EMA EU/3/19/2192 — include: EMA orphan feed identifies setmelanotide; designation status: Positive. Orphan designation is not marketing authorization.
EMA EU/3/19/2245 — include: EMA orphan feed identifies setmelanotide; designation status: Positive. Orphan designation is not marketing authorization.
EMA EU/3/18/2101 — include: EMA orphan feed identifies setmelanotide; designation status: Positive. Orphan designation is not marketing authorization.
EMA EU/3/16/1703 — include: EMA orphan feed identifies setmelanotide; designation status: Positive. Orphan designation is not marketing authorization.
EMA EU/3/16/1688 — include: EMA orphan feed identifies setmelanotide; designation status: Positive. Orphan designation is not marketing authorization.
ClinicalTrials.gov search
ClinicalTrials.gov name/alias discovery, including cited product names. Matches may concern combinations, background references or different formulations; identity and outcomes need screening.
30 retrieved · 0 included · 0 excluded · 30 awaiting a decision · 0 full-text appraisals
Registration is not evidence that a study succeeded, that results were published, or that a use is approved.
Other registries, unregistered studies and additional aliases remain outside this query.
Showing 25 of 30 record decisions, with included studies and unresolved records first. The versioned data inventory retains every record and study-family link.
ClinicalTrials.gov NCT06596135 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT05812183 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT03262610 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT03479437 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT03651765 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT05046132 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT03287960 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT02849977 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT06772597 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT02041195 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT03746522 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT04963231 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT05194124 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT04966741 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT05183802 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT02507492 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT02431442 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT03621007 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT05093634 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT06760546 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT03013543 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT01749137 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT07674290 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT04348175 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
ClinicalTrials.gov NCT01867437 — not screened: Registry name-query match awaiting intervention identity, study-family linkage and results appraisal.
Read the full Human Evidence Review
Supervised synthesis
What do selected human studies report about Setmelanotide?
A bounded review of sponsor-funded Phase 3 studies in rare genetic obesity syndromes: two small single-arm trials with withdrawal periods and one randomized trial followed by an open-label period.12
Bottom line from this bounded source set
The reviewed studies reported substantial weight reductions in some participants with specific genetic diagnoses. The cohorts were very small, and the Bardet-Biedl and Alström trial reported inconclusive results for the Alström subgroup.12
Reviewed study record
POMC- and LEPR-deficiency trials
Design
Two sponsor-funded, single-arm, open-label Phase 3 trials included a placebo-controlled withdrawal sequence for participants who first met a weight-loss threshold.1
Population
The trials enrolled ten participants with POMC-deficiency obesity and 11 with LEPR-deficiency obesity, all at least six years old.1
Outcomes reported
At approximately one year, at least 10% weight loss was reported for eight of ten participants in the POMC trial and five of 11 in the LEPR trial.1
Limitations
The cohorts were exceptionally small and lacked a parallel control group for the primary one-year endpoint; withdrawal eligibility also depended on an initial response.1
Reviewed study record
Bardet-Biedl and Alström syndrome trial
Design
A sponsor-funded Phase 3 trial began with a 14-week double-blind randomized placebo-controlled period and continued with a 52-week open-label period.2
Population
The trial randomized 38 participants aged six years or older with obesity and Bardet-Biedl syndrome or Alström syndrome.2
Outcomes reported
After 52 weeks of treatment, 32.3% of participants aged at least 12 years with Bardet-Biedl syndrome reached at least 10% weight reduction; results were reported as inconclusive for Alström syndrome.2
Limitations
The primary endpoint followed the open-label period, the syndrome-specific groups were small, and the reported result should not be generalized beyond the defined genetic populations.2
No registered Crossref update in the reviewed snapshotChecked August 19, 2026 for DOI 10.1016/s2213-8587(20)30364-8. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗
Publication update registered by CrossrefErratum ↗ · publisher metadata · February 1, 2023. Crossref metadata identifies the notice but does not by itself explain what wording changed.
Explore status sources, recent additions, and coverage gaps
Living status brief
What is the current status of Setmelanotide?
U.S. label record. The cited DailyMed label identifies Setmelanotide and contains the product's official indications and warnings. This profile links to the label without restating it as medical guidance.↗
The cited status sources were checked through July 22, 2026. This answer changes only through the profile’s visible version and correction history.
PeptideScanner currently has no selected safety records connected to this profile. That is a collection gap, not evidence that no such records exist.
PeptideScanner does not infer an answer where the cited records do not provide one. Open the source-linked records below to inspect their scope and limits.
This map describes PeptideScanner’s selected, source-linked collection. It is not an evidence grade and does not establish research quality, safety, effectiveness, or medical relevance.
6 exact source-declared trial-publication links connect selected NCT and PMID records. Open the exact graph →
PhasesPhase 3 3Phase 2 1Phase 4 1
Status at observationCompleted 2Recruiting 2Enrolling by invitation 1
A phase value is unavailable here for 9 selected records; this is not counted as “no phase.”
A status value is unavailable here for 9 selected records; this is not counted as a trial status.
PubMed bibliography
Publication composition
14 of 37 selected PubMed records include attributed title, venue, publication date, and publication-type fields.
Publication typesJournal Article 14Review 3Comment 2Research Support, Non-U.S. Gov't 2Clinical Trial 1Clinical Trial, Phase II 1Multicenter Study 1
Bibliography fields unavailable here for 23 selected records; the records remain visible as metadata observations.
Regulatory and publication surfaces
What is structurally connected?
Drugs@FDA applications
1
FDA Federal Register documents
4
DailyMed SPL versions
10
Canonical profile
Published
Profile structured data
Published
Linked dated records
66
Application counts reflect exact reviewed ingredient connections; Federal Register counts reflect exact reviewed peptide-name matches; DailyMed counts reflect listed SPL versions with retained ZIP receipts. “Published” describes this page’s indexing surface, not the state of scientific evidence.
These links come only from structured NCT and PMID identifiers declared by PubMed or ClinicalTrials.gov. They do not summarize the publications or establish findings.
PeptideScanner retained ClinicalTrials.gov record NCT06760546 at 2026-07-30T16:23:45.658Z. Its registry update date was 2026-02-12, and PeptideScanner's reviewed identity mapping was setmelanotide.
PeptideScanner retained ClinicalTrials.gov record NCT07674290 at 2026-07-30T16:19:03.062Z. Its registry update date was 2026-06-29, and PeptideScanner's reviewed identity mapping was setmelanotide.
DailyMed lists Structured Product Labeling version 1 for the reviewed Setmelanotide label family with a published date of 2020-12-16. PeptideScanner retained the exact versioned ZIP byte count and SHA-256 receipt without republishing its contents.
Counts and links describe PeptideScanner’s selected records. They are not rankings and do not establish research quality, safety, effectiveness, or medical relevance.
These links are based only on overlapping years and evidence lanes in PeptideScanner’s selected records. They do not imply that the peptides are medically or scientifically similar.
These dates come from selected source records and PubMed metadata. They are not a complete or continuous timeline of research, safety, approval, or effectiveness.
Evidence summary
What the cited records say
The cited DailyMed label identifies Setmelanotide and contains the product's official indications and warnings. This profile links to the label without restating it as medical guidance.↗
This is a source summary, not a medical recommendation. Status may differ by jurisdiction and product.
PeptideScanner retained ClinicalTrials.gov record NCT05093634 at 2026-08-13T05:52:27.024Z. Its registry update date was 2026-08-06, and PeptideScanner's reviewed identity mapping was setmelanotide.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 42498078 at 2026-08-10T10:49:10.787Z. PubMed recorded a metadata revision date of 2026-08-01 and an Entrez history date of 2026-07-24. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 42538728 at 2026-08-10T10:49:12.953Z. PubMed recorded a metadata revision date of 2026-08-01 and an Entrez history date of 2026-08-01. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 42008191 at 2026-08-10T10:49:08.851Z. PubMed recorded a metadata revision date of 2026-07-30 and an Entrez history date of 2026-04-20. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 42528856 at 2026-08-10T10:49:12.911Z. PubMed recorded a metadata revision date of 2026-07-30 and an Entrez history date of 2026-07-30. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 41894554 at 2026-08-10T18:13:44.905Z. PubMed recorded a metadata revision date of 2026-07-26 and an Entrez history date of 2026-03-27. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗
PeptideScanner retained ClinicalTrials.gov record NCT07496463 at 2026-08-10T18:10:04.219Z. Its registry update date was 2026-07-23, and PeptideScanner's reviewed identity mapping was setmelanotide.↗
PeptideScanner retained ClinicalTrials.gov record NCT06596135 at 2026-08-10T18:10:03.859Z. Its registry update date was 2026-07-15, and PeptideScanner's reviewed identity mapping was setmelanotide.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 42339090 at 2026-08-10T18:13:52.307Z. PubMed recorded a metadata revision date of 2026-07-14 and an Entrez history date of 2026-06-24. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 32213649 at 2026-08-10T18:13:32.288Z. PubMed recorded a metadata revision date of 2026-07-10 and an Entrez history date of 2020-03-28. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 42418774 at 2026-08-10T18:13:53.869Z. PubMed recorded a metadata revision date of 2026-07-09 and an Entrez history date of 2026-07-08. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗
PeptideScanner retained PubMed bibliographic metadata for PMID 42205046 at 2026-08-10T18:13:50.682Z. PubMed recorded a metadata revision date of 2026-07-06 and an Entrez history date of 2026-05-28. PeptideScanner associated this retained record with the identity slug setmelanotide. These dates describe PubMed metadata history, not the article's original publication date.↗