Biopharma Transcript

Grifols SA GRFS

Nasdaq · Phase 3 · hematology · biologic-other · EDGAR · Updated Oct 24, 2026

Grifols SA (Nasdaq: GRFS) is a hematology drug developer. Its lead program, Fibrinogen concentrate (BT524), is in Phase 3 for Congenital fibrinogen deficiency (US BLA approved 2025); acquired fibrinogen deficiency (EU approved, US Phase III to start 2026). Its next catalyst on record is Fibrinogen BT524: US commercial sales start (2026).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: Fibrinogen BT524 — US commercial sales start (2026). 3 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
Fibrinogen BT524Congenital fibrinogen deficiency (US); congenital and acquired deficiency (EU)biologic-otherApproved
Prolastin-C (alpha-1 proteinase inhibitor, IV) - SPARTAEmphysema due to congenital alpha-1 antitrypsin deficiencybiologic-otherApproved
Xembify (subcutaneous immunoglobulin)Secondary immunodeficiency in CLL, multiple myeloma and NHLbiologic-otherPhase 3
TrimodulinSevere community-acquired pneumonia (sCAP)biologic-otherPhase 3
Alpha-1 Proteinase Inhibitor SC 15%Emphysema due to congenital alpha-1 deficiency (subcutaneous)biologic-otherPhase 2
Immunoglobulin eye drops (Flebogamma DIF 5%)Dry eye diseasebiologic-otherPhase 2
ABvac40 (Araclon)Early-stage Alzheimer's disease (active vaccine against A-beta40)vaccinePhase 2
GIGA-2339 (GigaGen)Hepatitis B virus infectionantibodyPhase 1
GIGA-564 (GigaGen)Advanced solid tumorsantibodyPhase 1

For subscribers

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