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Drug · CHEMBL3545189

LANADELUMAB

7 sourcespipelines-2026-09-18-0.3.1

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ConductScience Library. LANADELUMAB. Drugs and targets, record CHEMBL3545189. Release pipelines-2026-09-18-0.3.1, 18 Sept 2026. https://conductscience.org/library/drugs/CHEMBL3545189

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Drug

Names and IDs as ChEMBL gives them, through Open Targets.

Name
LANADELUMAB
ChEMBL
ChEMBL ID
CHEMBL3545189
ChEMBL
Type
Antibody
ChEMBL
Brand names
Takhzyro
ChEMBL
Other names
DX-2930, Lanadelumab (shp643), Lanadelumab flyo, Lanadelumab-flyo, SHP-643, Tak-743
ChEMBL
Open Targets' highest stage
Approval, for 1 of its 3 diseases, from ATC, EMA Human Drugs, FDA and TTD
Open Targets

Targets1

The targets ChEMBL's mechanism records give for the drug, through Open Targets. A mechanism record says what the drug acts on, not how strongly.

TargetProteinMechanismActionGene in Genes
KLKB1Plasma kallikreinPlasma kallikrein inhibitorINHIBITORhttps://conductscience.org/library/genes/3818

Source ChEMBL

Diseases3

The diseases Open Targets' clinical reports study the drug for, the most trial reports first. The stage is Open Targets', the highest any of its sources reports for the pair, and each row names the sources that report it.

DiseaseOpen Targets' stageStage reported byReportsOf them trialsIts drugs
hereditary angioedemaApprovalATC, EMA Human Drugs, FDA and TTD73https://conductscience.org/library/drugs?q=MONDO_0019623
COVID-19Phase 3ClinicalTrials.gov33https://conductscience.org/library/drugs?q=MONDO_0100096
injuryPhase 1ClinicalTrials.gov11https://conductscience.org/library/drugs?q=MONDO_0021178

Trials22

Trials whose record names the drug by a name ChEMBL states, posted results first, then the largest. Open Targets read each trial's text to find its drugs.

TrialTitlePhaseParticipantsResults first postedNamed asLinked bySource
NCT04590586Study of Multiple Candidate Agents for the Treatment of COVID-19 in Hospitalized PatientsPhase 35152022-06-29lanadelumabIts nameClinicalTrials.gov
NCT02741596Long-term Safety and Efficacy Study of DX-2930 (SHP643) to Prevent Acute Angioedema Attacks in Patients With Type I and Type II HAEPhase 32122020-05-11lanadelumabIts nameClinicalTrials.gov
NCT03918239A Study to Determine the Bioavailability of Lanadelumab (SHP643) Administered Subcutaneously With the Prefilled Syringe and the Autoinjector in Healthy Adult Volunteer Participants.Phase 11902020-12-08lanadelumabIts nameClinicalTrials.gov
NCT02586805Efficacy and Safety Study of DX-2930 to Prevent Acute Angioedema Attacks in Patients With Type I and Type II HAEPhase 31252018-04-24DX-2930Its nameClinicalTrials.gov
NCT04206605A Study of Lanadelumab in Teenagers and Adults to Prevent Acute Attacks of Non-histaminergic Angioedema With Normal C1-Inhibitor (C1-INH)Phase 3772023-12-27lanadelumabIts nameClinicalTrials.gov
NCT04444895A Study of Long-Term Safety and Efficacy of Lanadelumab for Prevention of Acute Attacks of Non-histaminergic Angioedema With Normal C1-InhibitorPhase 3732024-06-17lanadelumabIts nameClinicalTrials.gov
NCT02093923A Double-Blind, Multiple Ascending Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DX-2930 in Hereditary Angioedema ParticipantsPhase 1382016-08-01lanadelumabIts nameClinicalTrials.gov
NCT03401671Study of Lanadelumab in Healthy Japanese and Matched Caucasian Adult SubjectsPhase 1322019-07-29lanadelumabIts nameClinicalTrials.gov
NCT05297786Hemodialysis.-Induced Hypotension Therapy for End Stage Kidney DiseasePhase 2282026-01-20lanadelumabIts nameClinicalTrials.gov
NCT04070326A Study of Lanadelumab to Prevent Hereditary Angioedema (HAE) Attacks in ChildrenPhase 3212022-05-26lanadelumabIts nameClinicalTrials.gov

1 to 10 of 22

See all 22 trials

Comparisons in its trials33

Comparisons Trial comparisons calculated in the trials whose record names the drug, most participants first. A comparison in one of its trials does not always compare the drug, so read the two groups.

ComparisonGroup 1, with the outcomeGroup 2, with the outcomeParticipantsTrialSource
Rollover Participants vs Non-rollover Participants: Number of Participants With Treatment-emergent Adverse Events (TEAEs)105 of 109101 of 103212NCT02741596Trial comparisons
Rollover vs Non-Rollover: deaths from any cause0 of 1090 of 103212NCT02741596Trial comparisons
Rollover vs Non-Rollover: serious adverse events12 of 1099 of 103212NCT02741596Trial comparisons
SHP643 Prefilled Syringe (PFS) vs SHP643 Autoinjector (AI): Number of Participants With Treatment-Emergent Adverse Events (TEAEs)19 of 9430 of 96190NCT03918239Trial comparisons
SHP643 Prefilled Syringe (PFS) vs SHP643 Autoinjector (AI): deaths from any cause0 of 940 of 96190NCT03918239Trial comparisons
SHP643 Prefilled Syringe (PFS) vs SHP643 Autoinjector (AI): serious adverse events2 of 942 of 96190NCT03918239Trial comparisons
Lanadelumab 300 mg vs Placebo: Number of Participants Achieving Attack-Free Status During the Treatment Period of Day 0 Through Day 1822 of 501 of 2777NCT04206605Trial comparisons
Lanadelumab 300 mg vs Placebo: deaths from any cause0 of 500 of 2777NCT04206605Trial comparisons
Lanadelumab 300 mg vs Placebo: serious adverse events7 of 501 of 2777NCT04206605Trial comparisons
Lanadelumab 300 mg vs Placebo: Number of Participants Achieving Attack-Free Status During the Presumed Steady State Period of Day 70 Through Day 1823 of 494 of 2776NCT04206605Trial comparisons

Papers from its trials13

The papers the trials whose record names the drug list on ClinicalTrials.gov as their results (RESULT) or as drawn from them (DERIVED), results first, newest first.

PMIDListed asTrials listing itSource
24980392RESULT1PubMed
42928084DERIVED1PubMed
40469312DERIVED2PubMed
39128590DERIVED1PubMed
37730089DERIVED1PubMed
37028510DERIVED2PubMed
36326435DERIVED1PubMed
36153561DERIVED2PubMed
34473343DERIVED1PubMed
34287942DERIVED1PubMed

Tests in its trials0

The tests ConductCognition runs that the trials whose record names the drug name in their registered outcomes, as ScienceGraph matched them. ConductCognition's list names the tests it runs, not every test a trial used.

None in this release.

Data dates

The date of each source this release read.

Open Targets
2026-09-18
Open Targets
ClinicalTrials.gov
2026-11-05
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
Papers the trials list, from Trials
2026-11-12
Trials
Comparisons, from Trial comparisons
2026-03-23
Trial comparisons
Tests named in the trials, as ScienceGraph matched them
2026-11-12
ConductCognition

Sources 7

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ConductCognition's list of its testsOur own data
  • ClinicalTrials.govNo license stated
  • NLM's MeSHNLM's terms
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ConductCognition's list of its testsOur own data: ConductCognition's list of its tests, https://conductcognition.com
  • ClinicalTrials.govnone stated
  • NLM's MeSHNLM's
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this drug from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/drugs/v1/CHEMBL3545189

GET https://conductscience.org/api/drugs/v1/CHEMBL3545189/trials?page=2