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Plate 345 of 545Verified

Fenfluramine

Also known asObedrex · Rotondin · Pesos · DL-Fenfluramine · Ponderax PA · Fenfluramina · Acino · Fenfluraminum

N-ethyl-1-[3-(trifluoromethyl)phenyl]propan-2-amine

PubChem CID
3337
Measurements
0
InChIKey
DBGIVFWFUFKIQN-UHFFFAOYSA-N

I · Summary

What is known

Published passages, each quoted whole and attributed to the database that published it. Two blocks are written here rather than quoted, and both say so where they stand: the synthesized summary at the top, which may draw only on the passages beneath it, and the history note, which cites the works it came from. Every claim in either carries a marker to its source.

How it acts

  • Dravet syndrome is a complex pediatric encephalopathy characterized by recurrent pharmacoresistant seizures of variable type, delayed development, and in many cases, impairment in speech, language, gait, and other neurocognitive functions. Despite substantial variation in presentation and severity, roughly 80% of patients with Dravet syndrome have mutations in the _SCN1A_ gene, which encodes the alpha subunit of a voltage-gated sodium channel (Nav1.1). This channel is predominantly localized in inhibitory GABAergic interneurons as well as in excitatory pyramidal neurons; it is thought that dysfunction of neurotransmission regulation results in the seizures and other corresponding symptoms of……
  • The exact mechanism of action of fenfluramine has not been clearly defined. Results of animal studies indicate that its appetite-inhibiting may result from stimulation of the ventromedial nucleus of the hypothalamus. The mechanism by which this stimulation is mediated has not yet been determined. Although fenfluramine is used in the treatment of obesity as an anorexigenic, it has not been firmly established that the pharmacologic action is principally one of appetite suppression; other CNS actions and/or metabolic effects may be involved. ... Cardiovascular and autonomic effects produced by fenfluramine in animals appear to be qualitatively similar to those of amphetamine, but as a pressor a…

    Hazardous Substances Data Bank (HSDB)McEvoy, G.K. (ed.). American Hospital Formulary Service - Drug Information 97. Bethesda, MD: American Society of Health-System Pharmacists, Inc. 1997 (Plus Supplements)., p. 1770

Behavior carries the pharmacological classes and the acute-effect durations, with plasma half-life kept separate from duration of effect.

History, discovery and cultural use

— Not in this archive. PubChem, ChEMBL and the Human Protein Atlas publish pharmacology, regulation and toxicology, and none of them publishes a heading for when Fenfluramine was first made, by whom, or how it has been used. That is a gap in the databases this site reads and not a gap in the literature — the history of these compounds is written, at length and under peer review, in the works below. This site does not summarize them; it says where they are. Where a published passage above happens to touch origin or traditional use, it appears inside the entry that carries it.

Histories of this field

Scholarship on psychedelics generally, not on Fenfluramine specifically. Whether any of these treats this compound is a question for the book, not for this page.

  • Mescaline: A Global History of the First Psychedelic

    Traces mescaline and the peyote and San Pedro cacti from pre-Columbian ritual use through nineteenth-century chemistry to twentieth-century psychiatry and the counterculture.

    Jay M. Mescaline: A Global History of the First Psychedelic. Yale University Press, New Haven and London; 2019. ISBN 9780300231076.

  • Expanding Mindscapes: A Global History of Psychedelicsopen access

    Essays on the international and cross-cultural history of psychedelic science, deliberately decentring the standard North American and European account.

    Dyck E, Elcock C, editors. Expanding Mindscapes: A Global History of Psychedelics. The MIT Press, Cambridge MA; 2023. ISBN 9780262546935 (paper), 9780262376891 (open access). doi:10.7551/mitpress/14417.001.0001.

  • Plants of the Gods: Their Sacred, Healing, and Hallucinogenic Powers

    Botany, ethnography and chemistry of the principal hallucinogenic plants, by the founder of modern ethnobotany and the chemist who first synthesized LSD.

    Schultes RE, Hofmann A, Rätsch C. Plants of the Gods: Their Sacred, Healing, and Hallucinogenic Powers. 2nd ed. Healing Arts Press, Rochester VT; 2001. ISBN 9780892819799.

  • Psychonauts: Drugs and the Making of the Modern Mind

    The tradition of scientific self-experimentation with psychoactive drugs, and its part in the emergence of psychology and of modernism.

    Jay M. Psychonauts: Drugs and the Making of the Modern Mind. Yale University Press, New Haven; 2023. ISBN 9780300257946.

  • Ancient Psychoactive Substances

    Archaeological and bioarchaeological evidence for psychoactive plant use across the ancient world.

    Fitzpatrick SM, editor. Ancient Psychoactive Substances. University Press of Florida, Gainesville; 2018. ISBN 9780813056708.

  • History and Current Status of Psychedelics and Entactogens for the Treatment of Psychiatric Disorders

    A chapter tracing psychedelic and entactogen research from earlier ritual use through the mid-century research period to current clinical trials.

    Stroud C, Posey Norris SM, Matney C, editors. History and Current Status of Psychedelics and Entactogens for the Treatment of Psychiatric Disorders. In: Exploring Psychedelics and Entactogens as Treatments for Psychiatric Disorders: Proceedings of a Workshop. National Academies Press, Washington DC; 2022. NBK587225.

    Workshop proceedings record what participants said; they are not a consensus statement of the National Academies.

  • Pharmacokinetic and Pharmacodynamic Aspects of Peyote and Mescaline: Clinical and Forensic Repercussions

    Peer-reviewed review covering the isolation, synthesis, pharmacology and ritual use of peyote and mescaline.

    Dinis-Oliveira RJ, Pereira CL, da Silva DD. Pharmacokinetic and Pharmacodynamic Aspects of Peyote and Mescaline: Clinical and Forensic Repercussions. Current Molecular Pharmacology 12(3):184–194; 2019. doi:10.2174/1874467211666181010154139.

Institutional archives

  • Heffter Research Institute Funds and coordinates clinical research on psilocybin, and keeps records of the studies it has supported since 1993. Sponsors the research it archives.
  • Multidisciplinary Association for Psychedelic Studies (MAPS) Sponsors clinical research, chiefly on MDMA-assisted therapy, and publishes an archive of historical and contemporary documents. A sponsor and an advocacy organization, not a disinterested archive; its clinical programme has a commercial arm.

The rest of this dossier

  • Toxicology — nothing published for Fenfluramine. An absent record is an absence of study, not evidence of safety.

Passages via PubChem descriptive sections, aggregating DrugBank, LiverTox, FDA, DEA, HSDB, EPA. Each is quoted whole and attributed to the database that published it. The only prose written here about Fenfluramine is the history note, which says so on its face and carries a reference for every claim in it.

II · Identity

Structure and descriptors

Descriptors are computed here with RDKit from the structure PubChem returns — not from the archive's stored copy, so an edited local structure cannot reach this table.

2D structural depiction of Fenfluramine
Depiction served by PubChem for CID 3337. Not redrawn here, so the picture and the identity come from the same record.
Formula
C12H16F3NR
Molecular weight
231.26g/molR
Exact mass
231.1235DaR
cLogP
3.25R
TPSA
12.0ŲR
H-bond donors
1R
H-bond acceptors
1R
Rotatable bonds
4R
Aromatic rings
1R
Heavy atoms
16R
Fraction sp³
0.500R
Formal charge
0R

Computed with RDKit 2025.09.2 from the SMILES returned by PubChem. Audit run 26/09/2026.

III · Behavior

Behavioral summary

Class, mechanism, and the duration of acute effects — each quoted from the record or trial that publishes it. Duration of effects and plasma half-life are shown separately, because they are different quantities and diverge by a factor of three or four.

Classification

Duration of acute subjective effects

—

No controlled human trial reporting a duration for this compound is cited here. The archive holds no other record of one either. A duration is not inferred from a chemical relative.

Plasma elimination half-life

How fast the body clears the drug — not how long the effects last. The two diverge sharply: LSD is cleared with a half-life of about 2.6 h while its subjective effects run 8–12 h.

  • Fenfluramine has an elimination half-life of 20 hours in healthy subjects.
    DrugBank
  • In one study, the mean elimination half-life of fenfluramine in patient with uncontrolled pH was about 20 hr while elimination half-life was about 11 hr when an acidic urinary pH was maintained. /Fenfluramine hydrochloride/
    Hazardous Substances Data Bank (HSDB)McEvoy, G.K. (ed.). American Hospital Formulary Service - Drug Information 97. Bethesda, MD: American Society of Health-System Pharmacists, Inc. 1997 (Plus Supplements)., p. 1770
  • Considerable first-pass effect due to rapid n-dealkylation of fenfluramine is apparent after per os doses. Rapid metabolism of derivative n-(2-benzoyloxyethyl)norfenfluramine has also been reported in man with apparent biological t/2 for total drug material of about 2 hr.
    Hazardous Substances Data Bank (HSDB)The Chemical Society. Foreign Compound Metabolism in Mammals Volume 3. London: The Chemical Society, 1975., p. 158
  • The half life of fenfluramine is 13 to 30 hours and is urine pH dependent. ...
    Hazardous Substances Data Bank (HSDB)Dart, R.C. (ed). Medical Toxicology. Third Edition, Lippincott Williams & Wilkins. Philadelphia, PA. 2004., p. 875

Primary pharmacological drivers

ChEMBL holds no curated mechanism-of-action record for this compound. The measured affinities below are the evidence this archive has for what it binds.

Mechanism, as published

Quoted verbatim from the database named after each passage, never summarized.

  • The neurochemical mechanisms by which drugs acting on central serotoninergic system modify feeding were reviewed. Fenfluramine, a clinically effective appetite suppressant, releases serotonin from nerve terminals and inhibits its reuptake, and considerable evidence suggests that these effects mediate its anorectic activity. The D isomer o…
    Hazardous Substances Data Bank (HSDB)PMID 2427023Garattini S et al; Appetite 7 Suppl: 15-38 (1986)
  • Dravet syndrome is a complex pediatric encephalopathy characterized by recurrent pharmacoresistant seizures of variable type, delayed development, and in many cases, impairment in speech, language, gait, and other neurocognitive functions. Despite substantial variation in presentation and severity, roughly 80% of patients with Dravet synd……
    DrugBank
  • The exact mechanism of action of fenfluramine has not been clearly defined. Results of animal studies indicate that its appetite-inhibiting may result from stimulation of the ventromedial nucleus of the hypothalamus. The mechanism by which this stimulation is mediated has not yet been determined. Although fenfluramine is used in the treat…
    Hazardous Substances Data Bank (HSDB)McEvoy, G.K. (ed.). American Hospital Formulary Service - Drug Information 97. Bethesda, MD: American Society of Health-System Pharmacists, Inc. 1997 (Plus Supplements)., p. 1770
  • Fenfluramine increases extracellular serotonin levels, and also acts as both a serotonergic 5-HT2 receptor agonist and σ1 receptor antagonist. These activities, through an incompletely understood mechanism, lead to anti-epileptiform activity and therapeutic benefit. This modulation has other effects such as decreased appetite, weight loss…
    DrugBank

IV · Clinical

Clinical description

Where this compound's substance class sits in ICD-11 and DSM-5-TR, and how much of the recorded literature speaks to each domain of a mental status examination.

No diagnostic chapter is shown for this compound. Either PubChem records no MeSH pharmacological class for it, or the class it records is not one of the substance classes ICD-11 gives a chapter to. Inferring a chapter from the compound’s name or its binding profile would be a diagnosis this archive is in no position to make.

How much has been written about each domain

The clinical domains, and how many of the records this archive holds for this compound say something under each. What the terms mean, and the word list behind every spoke, are set out in the method.

Affect0Mood1Perception0Cognition1Thought process0Thought content1Psychomotor activity1Insight and judgment0
This measures the literature, not the compound. Each spoke counts how many of the 8 records this archive holds for this compound say something under that domain — 1 at the widest ring. A long spoke means the subject has been written about, not that the effect is strong, and a spoke at the center means nothing here discusses it rather than that nothing happens. The terms behind each domain are listed in the method.
Mood 1
matched on “mood” · in Pharmacology: Pharmacodynamics
Cognition 1
matched on “cognitiv” · in Pharmacology: Mechanism of Action
Thought content 1
matched on “suicid” · in Pharmacology: Pharmacodynamics
Psychomotor activity 1
matched on “sedat” · in Pharmacology: Pharmacodynamics

VI · Profile

Affinity rosette

No measurement for Fenfluramine converts to an affinity at a molecular target, so there is no rosette to draw. This is an absence of data, not a finding about the compound.

VII · Toxicology

Toxicological profile

What has been measured, and what has been published — kept apart, and neither scored. There is no risk rating on this page; the archive once carried one, identical for every compound, produced by a stub.

Measured in this archive

Assays that bear on toxicity, drawn from the same ChEMBL records as everything else on this page. They are measurements of what a compound binds or does to cells — not verdicts about what it does to a person.

No hERG, cytochrome, cytotoxicity or transport measurement exists for Fenfluramine in this archive.

Published toxicology

— None. The toxicology databases this site reads — HSDB, RTECS and LiverTox, by way of PubChem — hold no record for Fenfluramine. They index compounds that have been studied for decades, so most of this archive has no entry. An absent record is an absence of study, not evidence of safety.

Published passages via PubChem toxicology sections, aggregating Hazardous Substances Data Bank (HSDB), RTECS, LiverTox. No figure on this page is scored, ranked or combined into a risk level.

VIII · Evidence

Every measurement

One row per published value. The identifier in the last column resolves to the ChEMBL assay record it was read from.

No bioactivity measurement is recorded for this compound in the archive.

P
PubChem
C
ChEMBL
R
Computed here with RDKit
D
Derived here from the stored measurement

IX · Trials

Registered clinical trials

Studies filed with ClinicalTrials.gov that name this compound as an intervention. A registered trial is a protocol, not a result — status and enrollment are printed beside every row, and withdrawn studies are counted rather than hidden.

24T

Registered studies

7T

Open or ongoing

21T

With a phase recorded

By phase

A study may carry two phase codes at once, so these count studies bearing each phase and do not sum to the total.

  • Phase 12
  • Phase 24
  • Phase 310
  • Phase 44
  • Not applicable1

By status

The registry’s own status for each record. Withdrawn and terminated studies are counted here rather than hidden — a stopped trial is part of what is known.

  • Completed10
  • Recruiting4
  • Terminated3
  • Unknown status2
  • Approved for marketing2
  • Not yet recruiting1
  • Enrolling by invitation1
  • Active, not recruiting1

Every matched study

Newest first by start date. Each identifier opens the registry record it came from; the title is the sponsor’s own, quoted.

  • NCT07503444Recruiting · Phase 3

    A Phase 3 Study of Fenfluramine Hydrochloride in Rett Syndrome

    Enrollment
    200Testimated
    Started
    2026-07-14
    Sponsor
    UCB BIOSCIENCES, Inc.

    Conditions Rett Syndrome

    Matched “Fenfluramine” in the study’s intervention “fenfluramine hydrochloride”

  • NCT07651293Not yet recruiting · Not applicable

    Using Fenfluramine to Test the Serotonin Deficiency Theory of Depression

    Enrollment
    46Testimated
    Started
    2026-07-01
    Sponsor
    Imperial College Healthcare NHS Trust

    Conditions Depression - Major Depressive Disorder

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine Hydrochloride”

  • NCT07555171Enrolling by invitation

    EEG Dynamics in Lennox-Gastaut Syndrome Patients Undergoing Fenfluramine Treatment

    Enrollment
    20Testimated
    Started
    2026-05-01
    Sponsor
    University of Chicago

    Conditions Lennox Gastaut Syndrome (LGS)

    Matched “Fenfluramine” in the study’s intervention “fenfluramine HCl”

  • NCT07112365Recruiting · Phase 4

    The FINTEPLA as an Anti-SUDEP Therapy in Dravet Syndrome Project

    Enrollment
    25Testimated
    Started
    2026-04-27
    Sponsor
    The University of Texas Health Science Center, Houston

    Conditions Dravet Syndrome

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine treatment (Fintepla)”

  • NCT06679413Completed · Phase 1

    A Study to Assess Drug-drug Interaction of ZX008 in Healthy Male and Female Study Participants

    Enrollment
    22Tactual
    Started
    2024-12-04
    Sponsor
    UCB BIOSCIENCES, Inc.

    Conditions Healthy Study Participants

    Matched “Fenfluramine” in the study’s intervention “fenfluramine HCl”

  • NCT06598449Recruiting · Phase 4

    Assessment of Safety of the Use of Fenfluramine in Children With Dravet Syndrome Under 24 Months of Age

    Enrollment
    5Testimated
    Started
    2024-10-22
    Sponsor
    University of Colorado, Denver

    Conditions Dravet Syndrome (DS) · Children Under 2 Years

    Matched “Fenfluramine” in the study’s intervention “fenfluramine”

  • NCT06118255Completed · Phase 3

    A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Fenfluramine (Hydrochloride) in Infants 1 Year to Less Than 2 Years of Age With Dravet Syndrome

    Enrollment
    25Tactual
    Started
    2024-05-21
    Sponsor
    UCB BIOSCIENCES, Inc.

    Conditions Dravet Syndrome

    Matched “Fenfluramine” in the study’s intervention “fenfluramine”

  • NCT04289467Recruiting · Phase 2

    Treatment of Refractory Infantile Spasms With Fenfluramine

    Enrollment
    10Testimated
    Started
    2023-06-16
    Sponsor
    Children's Hospital of Orange County

    Conditions Infantile Spasm

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine”

  • NCT05560282Terminated · Phase 3

    Fenfluramine for Adult Dravet Patients

    Enrollment
    7Tactual
    Started
    2023-01-11
    Sponsor
    University Health Network, Toronto

    Conditions Dravet Syndrome · Dravet Syndrome, Intractable

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine”

  • NCT05232630Unknown status · Phase 4

    Fenfluramine for the Treatment of Different Types of Developmental and Epileptic Encephalopathies: a Pilot Trial Exploring Epileptic and Non-epileptic Outcomes

    Enrollment
    20Testimated
    Started
    2022-10-20
    Sponsor
    Hospital Ruber Internacional

    Conditions Refractory Epilepsy · SYNGAP1 Encephalopathy · STXBP1 Encephalopathy With Epilepsy · Inv Dup(15) Encephalopathy · Multifocal or Bilateral Malformations of Cortical Development · Continuous Spike and Waves During Slow Sleep

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine”

  • NCT05064878Active, not recruiting · Phase 3

    A Phase 3 Study to Examine the Efficacy and Safety of ZX008 in Subjects With CDKL5 Deficiency Disorder.

    Enrollment
    87Tactual
    Started
    2022-03-08
    Sponsor
    Zogenix, Inc.

    Conditions CDKL5 Deficiency Disorder · Generalized Tonic Clonic Seizure · Epileptic Spasm · Refractory Seizures

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine”

  • NCT05026398Completed · Phase 4

    Fenfluramine and Cognition

    Enrollment
    56Tactual
    Started
    2021-04-12
    Sponsor
    University of Oxford

    Conditions Cognitive Function

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine”

  • NCT03861871Completed · Phase 2

    Fenfluramine in CDKL5 Deficiency Disorder (CDD)

    Enrollment
    7Tactual
    Started
    2019-10-29
    Sponsor
    NYU Langone Health

    Conditions CDD

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine Hydrochloride”

  • NCT03790137Completed · Phase 3

    Treatment of Sunflower Syndrome With ZX008 (Fenfluramine Hydrochloride) in Children and Young Adults (Ages 4-25).

    Enrollment
    20Tactual
    Started
    2019-05-31
    Sponsor
    Elizabeth Anne Thiele

    Conditions Photosensitive Epilepsy

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine Hydrochloride”

  • NCT03936777Completed · Phase 3

    A Study to Investigate the Long-Term Safety of ZX008 (Fenfluramine Hydrochloride) Oral Solution in Children and Adults With Epileptic Encephalopathy Including Dravet Syndrome and Lennox-Gastaut Syndrome

    Enrollment
    412Tactual
    Started
    2019-04-22
    Sponsor
    Zogenix, Inc.

    Conditions Dravet Syndrome · Lennox Gastaut Syndrome · Epileptic Encephalopathy

    Matched “Fenfluramine” in the study’s intervention “ZX008 (Fenfluramine Hydrochloride)”

  • NCT03299842Terminated · Phase 3

    A Study to Assess the Usability of the Embrace Seizure Detection Watch in Children and Young Adults With Dravet Syndrome

    Enrollment
    5Tactual
    Started
    2017-07-12
    Sponsor
    Zogenix International Limited, Inc., a subsidiary of Zogenix, Inc.

    Conditions Dravet Syndrome

    Matched “Fenfluramine” in the study’s intervention “ZX008 (Fenfluramine Hydrochloride)”

  • NCT02926898Completed · Phase 3

    A 2-Part Study to Investigate the Dose-Ranging Safety and Pharmacokinetics, Followed by the Efficacy and Safety of ZX008 (Fenfluramine Hydrochloride) Oral Solution as an Adjunctive Therapy in Children ≥ 2 Years Old and Young Adults With Dravet Syndrome

    Enrollment
    87Tactual
    Started
    2017-01-27
    Sponsor
    Zogenix International Limited, Inc., a subsidiary of Zogenix, Inc.

    Conditions Dravet Syndrome

    Matched “Fenfluramine” in the study’s intervention “ZX008 (Fenfluramine Hydrochloride)”

  • NCT02823145Completed · Phase 3

    An Open-Label Extension Trial to Assess the Long-Term Safety of ZX008 (Fenfluramine Hydrochloride HCl) Oral Solution in Children and Young Adults With Dravet Syndrome

    Enrollment
    375Tactual
    Started
    2016-06-08
    Sponsor
    Zogenix International Limited, Inc., a subsidiary of Zogenix, Inc.

    Conditions Dravet Syndrome

    Matched “Fenfluramine” in the study’s intervention “ZX008 (Fenfluramine Hydrochloride)”

  • NCT02682927Completed · Phase 3

    A Trial of Two Fixed Doses of ZX008 (Fenfluramine HCl) in Children and Young Adults With Dravet Syndrome

    Enrollment
    262Tactual
    Started
    2016-01-15
    Sponsor
    Zogenix International Limited, Inc., a subsidiary of Zogenix, Inc.

    Conditions Dravet Syndrome · Seizure Disorder

    Matched “Fenfluramine” in the study’s intervention “ZX008 (Fenfluramine Hydrochloride)”

  • NCT02655198Unknown status · Phase 2

    Add-on Therapy With Low Dose Fenfluramine in Lennox Gastaut Epilepsy

    Enrollment
    13Tactual
    Started
    2016-01
    Sponsor
    KU Leuven

    Conditions Epilepsy · Lennox Gastaut Syndrome

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine”

  • NCT00000506Completed · Phase 2

    Cardiovascular System in Obesity: Effect of Treatment

    Enrollment
    — no enrollment recorded in the registry entry
    Started
    1983-05
    Sponsor
    National Heart, Lung, and Blood Institute (NHLBI)

    Conditions Heart Diseases · Obesity · Vascular Diseases

    Matched “Fenfluramine” in the study’s intervention “fenfluramine”

  • NCT00000313Terminated · Phase 1

    Predictive Values of Serotonergic Alterations for Outcome - 2

    Enrollment
    0Tnot qualified
    Started
    — no start date recorded
    Sponsor
    National Institute on Drug Abuse (NIDA)

    Conditions Cocaine-Related Disorders

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine”

  • NCT04437004Approved for marketing

    Treatment of Dravet Syndrome With Fenfluramine (Expanded Access Protocol)

    Enrollment
    — no enrollment recorded in the registry entry
    Started
    — no start date recorded
    Sponsor
    University of California, Los Angeles

    Conditions Dravet Syndrome

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine”

  • NCT03780127Approved for marketing

    ZX008 Expanded Access Protocol

    Enrollment
    — no enrollment recorded in the registry entry
    Started
    — no start date recorded
    Sponsor
    Zogenix, Inc.

    Conditions Dravet Syndrome

    Matched “Fenfluramine” in the study’s intervention “Fenfluramine Hydrochloride”

Records from ClinicalTrials.gov (U.S. National Library of Medicine, NIH), API v2. A study is listed against a compound only when a verified name for that compound appears as a whole word in one of the study's own intervention names. A short code must appear as written, and a name the registry uses for something else (Aleph, a vaccine maker) is not matched. Title matches are not accepted. The matched name and the intervention text it matched are shown with every row.

Searched as Fenfluramine · DL-Fenfluramine · Ponderax PA. Run this search at the registry — it returns the unfiltered result, including studies this page rejected as belonging to a different molecule.

A registered trial is a protocol somebody filed with the registry. It is not a result, and nothing on this plate says whether Fenfluramine worked.

XI · Literature

Sources behind this dossier

The papers this compound's values were read from, ranked by what each contributed. Not a review of the field.

Every paper below is one some value on this page came from — a binding constant, a passage of pharmacology or toxicology, or a measured duration. Each entry says what this archive took from it. Nothing else is claimed about any of them: the title is the study’s own account of itself, and a summary written here would be an assertion with no source behind it.

  1. 01

    Neurochemical mechanism of action of drugs which modify feeding via the serotoninergic system

    Garattini S, Mennini T, Bendotti C et al. · Appetite 1986

    • · Mechanism of Action

    PMID 2427023