Big pharma · CSLLY · 260 trials led

CSL clinical trial pipeline

260 trials as lead sponsor, 17 recruiting now, 100 in phase 3. Live from ClinicalTrials.gov, updated daily.

  • Status changeStatus moved to completedWas recruiting · always alerts
  • Completion date movePrimary completion slipped 210 daysSlips and pull-ins of 30+ days
  • New trialNew trial registered in your scopeFirst posted within 30 days
  • Enrollment changeEnrollment grew to 1,200Moves of 15%+ or count finalised
  • Substantive record editPrimary endpoint redefined from 24 to 52 weeksRead overnight and flagged in plain English
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Archive historyOct 2022 to Jun 2026

145 recorded changes across CSL trials

Every status move, completion date shift and enrollment change ComplyRx has recorded across 34 of these trials. One is shown below.

Status changeStatus moved to active not recruiting from recruitingNCT06806657 · recorded 1 Jun 2026
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+141 more recorded changes · Track a drug to see every change the night it lands

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Most active programmes

The drugs appearing most often across CSL's recently active trials. Comparator arms are excluded.

  • CSL3126 trials
  • Patiromer5 trials
  • IgPro203 trials
  • CSL3002 trials
  • IgPro102 trials
  • AAV5-hFIX2 trials

Upcoming readouts

Next primary completion dates among CSL's active phase 2 and phase 3 trials. Dates are registry estimates and move often, which is exactly what the tracker watches.

Top therapeutic areas

Conditions studied most often across CSL's recently active trials.

  • Influenza, Human12 trials
  • Hemophilia B10 trials
  • Hyperkalemia5 trials
  • Hereditary Angioedema4 trials
  • Virus Diseases4 trials
  • Influenza4 trials

CSL trials

The 50 most significant of CSL's recently active trials, soonest estimated readout first.
Select any row for the full record; the change timeline unlocks with tracking.

TrialPhaseStabilityStatusEnrollmentEst. readout
Recombinant Single-chain Factor VIII (rVIII-SingleChain) in Chinese Participants With Hemophilia A Previously Treated With FVIII ProductsNCT06738485Recombinant single-chain factor VIII (rVIII-SingleChain)Phase 3Locked · track to revealOngoingActive, not recruiting60 est.26 Oct 2026
Efficacy and Safety of 4F-PCC (4-Factor Prothrombin Complex Concentrate) in Adult Patients Undergoing Complex Cardiovascular Surgery With Cardiopulmonary Bypass (CPB)NCT07094087BE1116Phase 3Locked · track to revealOngoingRecruiting200 est.18 Nov 2026
Recombinant Fusion Protein Linking Coagulation Factor IX With Albumin (rIX-FP) in Chinese Subjects With Hemophilia B Previously Treated With FIX TherapyNCT06399289Recombinant fusion protein linking coagulation factor IX with albumin (rIX-FP)Phase 3Locked · track to revealOngoingActive, not recruiting23 est.1 Dec 2026
A Phase 1b Study to Evaluate the PK of CSL300 (Clazakizumab) in Chinese Subjects With End Stage Kidney Disease (ESKD)NCT07619820CSL300Phase 1Not yet scoredOngoingRecruiting24 est.30 Aug 2027
Phase 3 Study of Fibrinogen Concentrate (CSL511) in Subjects With Pseudomyxoma Peritonei Undergoing Cytoreductive SurgeryNCT06617897CSL511 Fibrinogen concentrate (human)Phase 3Locked · track to revealOngoingRecruiting90 est.1 Sept 2027
Safety, Efficacy, and Pharmacokinetics of CSL889 in Adults and Adolescents With Sickle Cell Disease During Vaso-Occlusive CrisisNCT06699849CSL889Phase 2Locked · track to revealOngoingRecruiting70 est.22 Oct 2027
pHeNIxHizentra® in Inflammatory Neuropathies - pHeNIx StudyNCT04672733HizentraNot yet scoredOngoingRecruiting100 est.Dec 2027
OrPHEeObservatory of Patients With Haemophilia B Treated by IdElvion®NCT05086575Not yet scoredOngoingActive, not recruiting222 est.Dec 2027
Dose Range Finding, Efficacy, and Safety Study of Nebulized CSL787 in Adults With Non-cystic Fibrosis Bronchiectasis (NCFB)NCT07048262CSL787Phase 2Locked · track to revealOngoingRecruiting450 est.28 Feb 2028
Efficacy and Safety of Vamifeport in Adult Participants With Homeostatic Iron Regulator Gene (HFE)-Related Hereditary HemochromatosisNCT07332091VamifeportPhase 2Locked · track to revealOngoingRecruiting84 est.6 Mar 2028
Safety of Anumigilimab (CSL324) in Adults With Sickle Cell Disease (SCD)NCT07224360AnumigilimabPhase 2Locked · track to revealOngoingRecruiting63 est.29 Jun 2028
GREATA Study Investigating the Effectiveness and Safety of Garadacimab for Treating Patients With Hereditary Angioedema (HAE)NCT07001280Not yet scoredOngoingRecruiting200 est.31 Aug 2028
Efficacy and Safety of CSL222 (Etranacogene Dezaparvovec) Gene Therapy in Adults With Hemophilia B With Pretreatment Adeno-associated Virus Serotype 5 (AAV5) Neutralizing Antibodies (Nabs)NCT06003387CSL222 (AAV5-hFIXco-Padua)Phase 3Locked · track to revealOngoingRecruiting35 est.4 Oct 2028
Single-arm Study of IgPro20 in Adults With Secondary Immune Deficiencies Due to Hematologic Malignancies Treated With B-cell Targeting Chimeric Antigen Receptor T-cell and T-cell Redirecting TherapiesNCT07648264IgPro20Phase 3Not yet scoredOngoingNot yet recruiting63 est.16 Feb 2029
POSIBIL6ESKDCombined Dose-Finding and CV Outcomes Study With CSL300 (Clazakizumab) in Adult Subjects With ESKD Undergoing Dialysis (POSIBIL6ESKD)NCT05485961CSL300Phase 2Locked · track to revealOngoingRecruiting3,110 est.22 May 2029
Safety and Tolerability of Difelikefalin in Adolescents on Haemodialysis With Moderate-to-Severe PruritusNCT06593392DifelikefalinPhase 2Locked · track to revealOngoingRecruiting18 est.15 Aug 2029
Patiromer for Treatment of Hyperkalaemia in Children Under 12 Years of AgeNCT05766839PatiromerPhase 2Locked · track to revealOngoingRecruiting32 est.1 Dec 2029
Two Dose Levels of Privigen in Pediatric CIDPNCT03684018IgPro10Phase 4Locked · track to revealOngoingRecruiting30 est.20 Dec 2029
AvacostarAvacostar - (PASS)NCT05897684Not yet scoredOngoingRecruiting500 est.1 Dec 2030
Phase 4, Double-blind Study Evaluating the Response on Computed Tomography (CT) Lung Density Decline Rates of Respreeza / Zemaira Weekly for 3 Years in Adults With alpha1 Antitrypsin Deficiency (AATD)NCT07326592CE1226Phase 4Locked · track to revealOngoingNot yet recruiting270 est.15 Sept 2033
IX-TEND 3004Phase 3, Open-label, Single-dose Study of CSL222 in Adolescent Male Subjects (≥ 12 to < 18 Years of Age) With Severe or Moderately Severe Hemophilia BNCT07080905CSL222 (Adeno-associated viral vector serotype 5 [AAV5]-hFIXco-Padua)Phase 3Locked · track to revealOngoingRecruiting20 est.24 Oct 2033
IX-TEND 3003Long-term Follow-up Study of Male Adults With Hemophilia B Previously Treated With Etranacogene Dezaparvovec (CSL222)NCT05962398AAV5-hFIXco-PaduaNot yet scoredOngoingEnrolling by invitation56 est.23 Mar 2035
IX-TEND 4001An Observational Cohort Study to Characterize the Effectiveness and Safety of HEMGENIX® in Patients With Hemophilia BNCT06008938HEMGENIXNot yet scoredOngoingRecruiting500 est.1 Aug 2043
An Open-label, Multicenter Study to Assess the Pharmacokinetics (PK), Safety, and Tolerability of Subcutaneous IgPro20 in Immunoglobulin (IG) Treatment-naïve Participants With Primary Immunodeficiency (PID)NCT07076446IgProPhase 4Locked · track to revealCompleted8 est.30 Jun 2026
Safety Study in Subjects ≥ 12 Years of Age With Hereditary Angioedema Switching to GaradacimabNCT06806657GaradacimabPhase 4Locked · track to revealOngoingActive, not recruiting18 est.23 Jun 2026
A Clinical Study to Evaluate the Efficacy, Safety and Immunogenicity of an Adjuvanted Influenza Vaccine Compared to a Non-adjuvanted Influenza Vaccine in Adults ≥65 Years of AgeNCT06087640aQIV or aTIVPhase 3Locked · track to revealCompleted38,769 est.26 May 2026
Study of AAV5-hFIX in Severe or Moderately Severe Haemophilia BNCT05360706AAV5-hFIXNot yet scoredCompleted9 est.26 Mar 2026
MODULAATEThe Safety and Efficacy of Alpha-1 Antitrypsin (AAT) for the Prevention of Graft-versus-host Disease (GVHD) in Patients Receiving Hematopoietic Cell TransplantNCT03805789AATPhase 2Locked · track to revealCompleted222 est.19 Mar 2026
First-In-Human Study To Evaluate The Safety, Tolerability, Pharmacokinetics, And Pharmacodynamics Of Escalating Single And Multiple Doses Of CSL040 In Healthy SubjectsNCT05937581CSL040Phase 1Locked · track to revealCompleted62 est.4 Dec 2025
Long-term Safety and Efficacy of CSL312 (Garadacimab) in the Prophylactic Treatment of Hereditary Angioedema AttacksNCT04739059CSL312Phase 3Locked · track to revealCompleted171 est.21 Nov 2025
CSL312_3003 Safety and Pharmacokinetic Study in Subjects 2 to 11 Years of Age With Hereditary AngioedemaNCT05819775CSL312Phase 3Locked · track to revealCompleted22 est.19 Nov 2025
Patiromer JADETrial Evaluating the Efficacy and Safety of Patiromer in Chinese SubjectsNCT05136664Patiromer Powder for Oral Suspension (Part A)Phase 3Locked · track to revealCompleted262 est.18 Nov 2025
Effect of Food on the Oral Bioavailability of a Prolonged-release Formulation of Vamifeport in Healthy AdultsNCT06996184Vamifeport (PR formulation)Phase 1Locked · track to revealCompleted28 est.1 Jul 2025
Double-blind, Randomized, Placebo-controlled Study Evaluating Efficacy and Safety of IgPro20 in Post-COVID-19 POTSNCT06524739IgPro20Phase 3Locked · track to revealStoppedTerminated16 est.20 Jun 2025
Pharmacokinetics and Pharmacodynamics of Two Prolonged-release Formulations of Vamifeport in Healthy AdultsNCT06726863Vamifeport IRFPhase 1Locked · track to revealCompleted22 est.27 Jan 2025
OPERARegister of Patients With haEmophilia A tReated With Afstyla®NCT04675541Afstyla®Not yet scoredCompleted62 est.31 Dec 2024
RECLAIIMA Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of IgPro20 in Adults With Dermatomyositis (DM)NCT04044690human immunoglobulin GPhase 3Locked · track to revealStoppedTerminated134 est.2 Dec 2024
Study to Evaluate Immunogenicity, Safety and Tolerability of Adjuvanted and Non-Adjuvanted H2N3 Influenza Vaccines in AdultsNCT05875961Low dose A/H2N3c + standard dose MF59Phase 1Locked · track to revealCompleted600 est.15 Nov 2024
Evaluation of BE1116 in Patients With Traumatic Injury and Acute Major Bleeding to Improve Survival ( TAP Study )NCT05568888BE1116Phase 3Locked · track to revealStoppedTerminated1,366 est.29 Oct 2024
Safety, Reactogenicity, and Immunogenicity Study of a Self-Amplifying MRNA Influenza Vaccine in Healthy AdultsNCT06028347sa-mRNA vaccine Dose 1Phase 1Locked · track to revealCompleted96 est.13 Oct 2024
Phase 3 Study of Difelikefalin in Haemodialysis Chinese Adult Subjects With Moderate-to-Severe PruritusNCT05885737Difelikefalin InjectionPhase 3Locked · track to revealCompleted260 est.25 Sept 2024
AmAREtTIRespreeza® Self-administration and Learning Program (AmAREtTI Study)NCT04262284Not yet scoredCompleted15 est.6 May 2024
Study to Evaluate Safety and Immunogenicity of Different Priming and Booster Regimens With Adjuvanted H5N8 and/or H5N6 Influenza Vaccine in AdultsNCT05874713aH5N8c on Day 1Phase 2Locked · track to revealCompleted480 est.25 Apr 2024
IMAGINEClazakizumab for the Treatment of Chronic Active Antibody Mediated Rejection in Kidney Transplant RecipientsNCT03744910ClazakizumabPhase 3Locked · track to revealStoppedTerminated194 est.8 Apr 2024
ViSionSerenityStudy to Assess Efficacy and Safety of VIT-2763 (Vamifeport) in Subjects With Sickle Cell DiseaseNCT04817670VIT-2763 120 mgPhase 2Locked · track to revealCompleted25 est.7 Mar 2024
The Celljuvant Study: A Phase 3 Immunogenicity and Safety Study of aQIVc Vaccine in Adults Aged 50 Years and OlderNCT06015282Investigational aQIVcPhase 3Locked · track to revealCompleted7,741 est.5 Mar 2024
CARE-HKCardiovascular and Renal Treatment in Heart Failure Patients With Hyperkalaemia or at High Risk of HyperkalaemiaNCT04864795Not yet scoredCompleted2,636 est.29 Feb 2024
PORTRAYRAYALDEE Non Interventional Study (NIS) on Effectiveness in ND-CKD SHPT PatientsNCT05460234Not yet scoredCompleted110 est.31 Jan 2024
ReliefCensusCross-sectional Study to Assess Prevalence and Burden of CKD-associated Pruritus in Haemodialysis PatientsNCT05524467Not yet scoredCompleted3,100 est.31 Jan 2024
Garadacimab Safety, Pharmacokinetics, and Pharmacodynamics in Idiopathic Pulmonary FibrosisNCT05130970GaradacimabPhase 2Locked · track to revealCompleted81 est.2 Jan 2024
View all trials260

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We check every one of its trials daily and tell you what moved.

  • Status changeStatus moved to completedWas recruiting · always alerts
  • Completion date movePrimary completion slipped 210 daysSlips and pull-ins of 30+ days
  • New trialNew trial registered in your scopeFirst posted within 30 days
  • Enrollment changeEnrollment grew to 1,200Moves of 15%+ or count finalised
  • Substantive record editPrimary endpoint redefined from 24 to 52 weeksRead overnight and flagged in plain English
US registryClinicalTrials.gov
EU registryCTIS · Soon
260

Trials as lead sponsor

17

Recruiting now

100

Phase 3 trials

69

Phase 2 trials

45

Phase 1 trials

27

Phase 4 trials