Big pharma · GRFS · 100 trials led

Grifols clinical trial pipeline

100 trials as lead sponsor, 5 recruiting now, 42 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

77 recorded changes across Grifols trials

Every status move, completion date shift and enrollment change ComplyRx has recorded across 17 of these trials. One is shown below.

Enrollment changeEnrollment finalised at 0NCT02472665 · recorded 1 Jun 2026
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+73 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 Grifols's recently active trials. Comparator arms are excluded.

  • Standard Medical Treatment6 trials
  • Alpha-1 MP5 trials
  • Trimodulin3 trials
  • IGSC 20%3 trials
  • Fibrin Sealant Grifols3 trials
  • GAMUNEX-C3 trials

Upcoming readouts

Next primary completion dates among Grifols'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 Grifols's recently active trials.

  • COVID-197 trials
  • Primary Immunodeficiency6 trials
  • Alpha1-Antitrypsin Deficiency3 trials
  • Congenital Afibrinogenemia3 trials
  • Multiple Myeloma3 trials
  • Hepatitis B, Chronic3 trials

Grifols trials

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

TrialPhaseStabilityStatusEnrollmentEst. readout
SPARTAEfficacy and Safety of Alpha1-Proteinase Inhibitor (Human), Modified Process (Alpha-1 MP) in Subjects With Pulmonary Emphysema Due to Alpha1 Antitrypsin Deficiency (AATD)NCT01983241Alpha-1 MPPhase 3Locked · track to revealOngoingActive, not recruiting345 est.Aug 2026
SWIFT-SCA Non-inferiority Pharmacokinetic and Safety/Tolerability Study of Two Different Doses of Weekly SC Alpha1-PI 15% Compared With Corresponding Standard IV Alpha1-PI in Participants With Alpha1-Antitrypsin Deficiency (AATD)NCT07555483Alpha-1 15%Phase 3Locked · track to revealOngoingRecruiting40 est.30 Sept 2027
XPERTA Study to Evaluate the Pharmacokinetics and Safety of XEMBIFY Versus Gamunex-C in Participants With Chronic Inflammatory Demyelinating PolyradiculoneuropathyNCT07540221Gamunex-CPhase 3Locked · track to revealOngoingRecruiting40 est.31 Dec 2027
ESsCAPEEfficacy and Safety of Trimodulin (BT588) in Subjects With Severe Community-acquired Pneumonia (sCAP)NCT05722938TrimodulinPhase 3Locked · track to revealOngoingRecruiting590 est.31 Jul 2028
SIGMAA Clinical Trial to Evaluate Efficacy, Safety, and Pharmacokinetics of Gamunex in Participants With Chronic Lymphocytic Leukemia, Multiple Myeloma, or Non-Hodgkin LymphomaNCT07582432Gamunex-C, 10% Injectable SolutionPhase 3Locked · track to revealOngoingRecruiting49 est.31 Aug 2028
SPARTA-OLELong Term Safety of Alpha1-Proteinase Inhibitor in Subjects With Alpha1 Antitrypsin DeficiencyNCT02796937Alpha-1 MPPhase 3Locked · track to revealOngoingEnrolling by invitation290 est.Sept 2028
Efficacy of Alphanate FVIII/VWF Concentrate in Type 3 Von Willebrand PatientsNCT00555555Alphanate SD/HTPhase 4Locked · track to revealOngoingActive, not recruiting15 est.Dec 2028
Safety, Pharmacokinetics and Efficacy of an ATIII ConcentrateNCT00319228Plasma-derived AT-III concentratePhase 2Locked · track to revealOngoingActive, not recruiting30 est.Dec 2028
Evaluating the Safety, Tolerability, and Efficacy of GRF312 5% in Participants With Dry Eye Disease (DED).NCT07264517GRF312 5%Phase 2Locked · track to revealCompleted103 est.20 May 2026
EXCELLA Study to Evaluate Efficacy, Safety, and PK of XEMBIFY®+Standard Medical Treatment (SMT) Compared to Placebo+SMT to Prevent Infections in Participants With HGG and Recurrent or Severe Infections Associated With B-cell Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin LymphomaNCT05645107XembifyPhase 3Locked · track to revealOngoingRecruiting386 est.May 2026
A Study to Evaluate Safety, Tolerability and Pharmacokinetics of Two Different Doses of Alpha1-Proteinase Inhibitor Subcutaneous (Human) 15% in Participants With Alpha1-Antitrypsin DeficiencyNCT04722887Alpha-1 15%Phase 1Locked · track to revealCompleted17 est.1 Aug 2025
TRICOVIDEfficacy and Safety of Trimodulin (BT588) in Subjects With CAP Including COVID-19 PneumoniaNCT05531149TrimodulinPhase 3Locked · track to revealStoppedTerminated107 est.5 May 2025
APACHEShort-term Survival of Subjects With Acute-on-chronic Liver Failure After Plasma Exchange With Human Serum Albumin 5%NCT03702920SMT + PE-A 5%Phase 3Locked · track to revealStoppedTerminated274 est.14 Apr 2025
FIB Grifols Congenital Deficiency for On-demand Treatment and Surgical ProphylaxisNCT04636268FIB GrifolsPhase 3Locked · track to revealStoppedWithdrawn0 est.Mar 2025
Efficacy and Safety of Fanhdi®, a High-purity Von Willebrand Containing FVIII Concentrate, in Pediatric Patients With Von Willebrand DiseaseNCT02472665plasma-derived FVIII/VWF concentratePhase 4Locked · track to revealStoppedWithdrawn0 est.10 Dec 2024
PRECIOSAEffects of Long-Term Administration of Human Albumin in Participants With Decompensated Cirrhosis and AscitesNCT03451292Albutein 20%Phase 3Locked · track to revealCompleted410 est.21 May 2024
PreCyssionPrevention of Maternal-fetal Cytomegalovirus Transmission After Primary Maternal Infection, GW ≤ 14 (PreCyssion)NCT05170269BT097Phase 3Locked · track to revealStoppedTerminated48 est.19 Nov 2023
AdFIrstAdjusted Fibrinogen Replacement StrategyNCT03444324BT524Phase 3Locked · track to revealCompleted222 est.25 Sept 2023
FORCEStudy of the Efficacy and Safety of Immune Globulin Intravenous (Human) Flebogamma® 5% Dual Inactivation and Filtration (DIF) in Participants With Post-polio SyndromeNCT02176863Flebogamma® 5% DIFPhase 2Locked · track to revealStoppedTerminated191 est.24 Nov 2022
A Study to Evaluate IGSC 20% Biweekly Dosing in Treatment-Experienced Participants and Loading/Maintenance Dosing in Treatment-Naïve Participants With Primary ImmunodeficiencyNCT04566692IGSC 20%Phase 4Locked · track to revealCompleted33 est.18 Jul 2022
Safety and Efficacy of USB002 for Respiratory Distress Due to COVID-19NCT04778059USB002Phase 2Locked · track to revealStoppedTerminated21 est.10 May 2022
A Study of Safety and Efficacy of Fibrin Sealant Grifols as an Adjunct to Haemostasis During Surgery in Paediatric ParticipantsNCT03461406Fibrin Sealant GrifolsPhase 3Locked · track to revealCompleted186 est.15 Apr 2022
A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Immune Globulin (Human) 10% (Gamunex-C) PEG Process (IVIG-PEG) Compared to Gamunex-C in Participants With Primary Humoral ImmunodeficiencyNCT04561115Gamunex-CPhase 3Locked · track to revealCompleted33 est.28 Mar 2022
Study to Evaluate the Safety and Efficacy of Liquid Alpha1-Proteinase Inhibitor (Human) in Hospitalized Participants With Coronavirus Disease (COVID-19)NCT04547140Liquid Alpha1-Proteinase Inhibitor (Human)Phase 2Locked · track to revealStoppedTerminated57 est.13 Dec 2021
COVID-19A Study to Evaluate the Safety and Efficacy of C19-IG 20% in SARS-CoV-2 Infected Asymptomatic Ambulatory OutpatientsNCT04847141C19-IG 20%Phase 3Locked · track to revealStoppedTerminated465 est.10 Nov 2021
Study to Evaluate the Safety and Efficacy of High Dose Intravenous Immune Globulin (IVIG) Plus Standard Medical Treatment (SMT) Versus SMT Alone in Participants in Intensive Care Unit (ICU) With Coronavirus Disease (COVID-19)NCT04480424GAMUNEX-CPhase 2Locked · track to revealCompleted100 est.25 Aug 2021
ESsCOVIDEfficacy and Safety of Trimodulin in Subjects With Severe COVID-19NCT04576728TrimodulinPhase 2Locked · track to revealCompleted166 est.29 Jun 2021
Study to Evaluate the Safety and Efficacy of Prolastin in Hospitalized Subjects With COVID-19NCT04495101ProlastinPhase 2Locked · track to revealCompleted100 est.26 Apr 2021
Study to Evaluate the Safety and Efficacy of High Dose IVIG in Hospitalized Participants With Coronavirus Disease (COVID-19)NCT04432324Intravenous Immune GlobulinPhase 2Locked · track to revealCompleted100 est.3 Mar 2021
Long-term Safety of Alpha1-Proteinase Inhibitor (Human) in Japanese Subjects With Alpha1 Antitrypsin Deficiency (GTI1401-OLE)NCT02870348Alpha-1 MPPhase 1Locked · track to revealCompleted4 est.16 Feb 2021
A Study to Evaluate Safety and Efficacy of Convalescent Methylene Blue Treated (MBT) Plasma From Donors Recovered From Coronavirus Disease 2019 (COVID-19)NCT04547127Convalescent anti-SARS-CoV-2 MBT PlasmaPhase 2Locked · track to revealCompleted200 est.4 Feb 2021
Alphanate in Immune Tolerance Induction TherapyNCT03095287AlphanatePhase 2Locked · track to revealStoppedTerminated2 est.18 Sept 2020
Study Evaluating IGSC 20% Flexible Dosing in Treatment-Experienced and Treatment-Naive Subjects With Primary ImmunodeficiencyNCT03814798IGSC 20% daily push versus every 2 weeks pumpPhase 3Locked · track to revealStoppedWithdrawn0 est.Sept 2020
Pharmacokinetic, Efficacy and Safety of BT524 in Patients With Congenital Fibrinogen DeficiencyNCT02065882BT524 (Part I)Phase 3Locked · track to revealCompleted67 est.18 May 2020
Study to Investigate Efficacy, Safety and Pharmacokinetics of BT595 in Subjects With PIDNCT02810444IgG Next Generation (BT595)Phase 3Locked · track to revealCompleted81 est.1 Apr 2020
IG0902Pharmacokinetics, Efficacy, and Safety of Human Plasma-Derived Fibrinogen (FIB Grifols) in Participants With Congenital AfibrinogenemiaNCT02281500Human Plasma-Derived Fibrinogen ConcentratePhase 1Locked · track to revealCompleted24 est.11 Nov 2019
Efficacy and Safety of Plasma Exchange With Albutein® 5% in Participants With Amyotrophic Lateral SclerosisNCT02872142Albutein 5%Phase 2Locked · track to revealCompleted12 est.15 Aug 2019
Efficacy, Pharmacokinetics, Safety, and Tolerability of IGSC 20% in Subjects With Primary ImmunodeficiencyNCT02806986IGSC 20%Phase 3Locked · track to revealCompleted61 est.15 May 2019
Efficacy and Safety of IGIV-C in Corticosteroid Dependent Patients With Generalized Myasthenia GravisNCT02473965IGIV-CPhase 2Locked · track to revealCompleted60 est.Feb 2019
This Clinical Study is to Test Efficacy and Safety of BT595 in Chronic Primary Immune Thrombocytopenia (ITP)NCT02859909BT595Phase 3Locked · track to revealCompleted34 est.Dec 2018
Safety Study of Alphanate in Previously Treated Patients With Severe Hemophilia ANCT00323856Alphanate SD/HTPhase 4Locked · track to revealCompleted51 est.11 Dec 2018
Study of the Safety of USB005 in Healthy VolunteersNCT03615196USB005 (aclerastide) Ophthalmic SolutionPhase 1Locked · track to revealCompleted32 est.8 Nov 2018
BT062 in Combination With Lenalidomide or Pomalidomide and Dexamethasone in Patients With Multiple MyelomaNCT01638936BT062 , intravenous administrationPhase 1Locked · track to revealCompleted64 est.30 Oct 2018
GamaSTANAnti-Hepatitis A Virus, Pharmacokinetics, and Safety of Immune Globulin (Human)NCT03351933Immune Globulin (Human)Phase 4Locked · track to revealCompleted28 est.27 Apr 2018
A Study to Assess the Efficacy and Safety of IGIV-C in Patients With Myasthenia Gravis ExacerbationsNCT02413580IGIV-CPhase 3Locked · track to revealCompleted49 est.Apr 2018
AMBARA Study to Evaluate Albumin and Immunoglobulin in Alzheimer's DiseaseNCT01561053Albumin 5%Phase 2Locked · track to revealCompleted347 est.6 Mar 2018
Safety and Efficacy of Preoperative Antithrombin Supplementation in Patients Undergoing High-Risk Cardiopulmonary BypassNCT02037555AT-III (Human)Phase 2Locked · track to revealCompleted425 est.25 Jan 2018
A Study to Evaluate the Efficacy and Safety of IGIV-C in Symptomatic Subjects With Generalized Myasthenia GravisNCT02473952IGIV-CPhase 2Locked · track to revealCompleted62 est.Jan 2018
BT063 in SLEProof-of-Concept Study With BT063 in Subjects With Systemic Lupus ErythematosusNCT02554019BT063Phase 2Locked · track to revealCompleted36 est.25 Oct 2017
Safety and Pharmacokinetics of IGSC 20% in Subjects With Primary ImmunodeficiencyNCT02604810IGIV-C 10%Phase 3Locked · track to revealCompleted53 est.Sept 2017
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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
100

Trials as lead sponsor

5

Recruiting now

42

Phase 3 trials

48

Phase 2 trials

13

Phase 1 trials

9

Phase 4 trials