Evidence review: Open Peptide Project (verified against primary PubMed, ClinicalTrials.gov & FDA records) · Last checked 2026-10-27. ← Back to Evidence Library

Histrelin (Supprelin LA; Vantas discontinued): what the evidence says

At a glance

What it is: a synthetic 9-amino-acid GnRH analog released from a small implant placed under the skin of the upper arm. Approved as Supprelin LA (May 2007) for central precocious puberty in children. A version for prostate cancer (Vantas) was also approved but is now listed as discontinued. R1, R2, R3

What the evidence says: 馃煥 in a single-arm trial of 36 children with central precocious puberty, the implant kept puberty hormones suppressed. R4 In men with prostate cancer, testosterone stayed suppressed in long-term open-label use. R5

Biggest risks: implant-site reactions were very common (51.1%); the label also warns about an early hormone surge, implant breakage, psychiatric events, seizures, severe skin reactions and raised pressure in the skull. Prohibited in male athletes. R3, R6

Rating

Human Human evidence Moderate: single-arm trials plus long-term follow-up R4, R5
Animal Animal / lab evidence Not reviewed
Regulatory FDA-approved R1 路 not on FDA's 503A or 503B bulk-substance category lists and not on FDA's compounding safety-risk page R7, R8, R9 路 prohibited in male athletes (WADA S2.2.1) R6
Established human dose Yes, label dose (see Study details)

Evidence verdict: Central precocious puberty: Moderate (approved; single-arm trial) 路 Prostate cancer: Moderate (approved as Vantas, now discontinued) 路 Off-label hormone use: No human data

This page reports what studies used. It is not dosing advice.

Legend: HUMAN data 路 ANIMAL / LAB data 路 UNKNOWN 路 UNVERIFIED: not yet confirmed against a primary source

About the evidence: objective hormone endpoints, but no randomized comparisons in the trials reviewed.

What is it?

Related pages: goserelin, nafarelin, leuprolide, triptorelin.

Does it work?

Is it safe?

Gray-market vials: extra risks

A gray-market vial has no quality control and no guarantee of identity, strength or sterility. We test retail vials blind under the Open Peptide Standard; see /tests/. A passing test covers one batch on one date and does not mean the compound is safe.

Is it legal?

Study details
Study details

These are amounts researchers used, not recommendations.

Study People / model Route Amount used Follow-up Reported Citation
Eugster 2007 (phase 3, open-label) 36 children with CPP SC implant Per label 12 months LH suppressed PMID 17327379
Shore 2012 (open-label extension) 104 men with advanced prostate cancer SC implant Per study Up to 4+ years Testosterone suppressed; hot flashes 64.4% PMID 21851539

Full reference list (PubMed, CT.gov, FDA and WADA checked Oct 27, 2026)

  1. R1 Drugs@FDA, Supprelin LA (histrelin), application NDA022058 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA022058
  2. R2 Drugs@FDA, Vantas (histrelin), application NDA021732 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA021732
  3. R3 Supprelin LA prescribing information, label published Sep 25, 2025 (DailyMed, checked Oct 27, 2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8fb000e-3cc9-4803-b71d-2cc597661977
  4. R4 Eugster EA, et al. J Clin Endocrinol Metab. 2007. PMID 17327379
  5. R5 Shore N, et al. BJU Int. 2012. PMID 21851539
  6. R6 WADA. The 2026 Prohibited List, S2.2.1, Chorionic Gonadotrophin and Luteinizing Hormone and their releasing factors, naming goserelin, histrelin and nafarelin among the GnRH analogues (prohibited in males). https://www.wada-ama.org/sites/default/files/2025-09/2026list_en_final_clean_september_2025.pdf
  7. R7 FDA, 503A bulk drug substances categories list (updated May 14, 2026). https://www.fda.gov/media/94155/download
  8. R8 FDA, 503B bulk drug substances categories list (updated Mar 21, 2025). https://www.fda.gov/media/94164/download
  9. R9 FDA, Certain bulk drug substances for use in compounding that may present significant safety risks (content current Apr 22, 2026). https://www.fda.gov/drugs/human-drug-compounding/certain-bulk-drug-substances-use-compounding-may-present-significant-safety-risks

Disclaimer

This page is for education and harm reduction, not medical advice or a recommendation to use Histrelin (Supprelin LA; Vantas discontinued). This is a prescription medicine. Use it only under the care of a licensed clinician; do not buy it from research-chemical or gray-market sellers. Report problems to FDA MedWatch (https://www.fda.gov/safety/medwatch).