Skip to main content

motixafortide

Generic: MOTIXAFORTIDE ACETATE·Brand: APHEXDA, Aphexda

motixafortide: 4 clinical trials tracked.

motixafortide evidence translation

What we can confirm

4 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about motixafortide, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 1 study sponsors
Clinical Trials (4)

Prevent Allergic Reactions to Aphexda With Dexamethasone (PARADE)

NCT07101445·Phase 4·FLNA
Recruiting

Primary endpoint: Incidence and severity of systemic reactions

InterventionalRandomizedtriple94 targetStarted 2025-09Completion 2027-121 site · United StatesEmory University

Sickle Cell Disease Stem Cell Mobilization and Apheresis Using Motixafortide

NCT06442761·Phase 1
Recruiting

Primary endpoint: To assess the safety and tolerability of motixafortide in participants with sickle cell disease (SCD) as determined by the incidence of adverse events.

Interventionalopen15 targetStarted 2024-11Completion 2028-073 sites · United StatesSt. Jude Children's Research Hospital

A Pharmacodynamic Study of the Apheresis Product of Multiple Myeloma Patients Undergoing Quad-induction Followed by Motixafortide + G-CSF Mobilization

NCT06547112·Phase 1
Completed

Primary endpoint: Absolute number and relative proportions of CD34+ cell subsets by extended immunophenotypic profiling using multicolor fluorescence activated cell sorting (mFACS) on the apheresis product

Interventionalopen20 enrolledStarted 2024-10Completion 2025-081 site · United StatesWashington University School of Medicine

A Pilot Safety and Feasibility Study to Evaluate Motixafortide (CXCR4/SDF-1 Inhibition) and Natalizumab (VLA-4/VCAM-1 Inhibition) as a Novel Regimen to Mobilize CD34+ Hematopoietic Stem Cells for Gene Therapies in Sickle Cell Disease (SCD)

NCT05618301·Phase 1
Completed

Primary endpoint: Safety and tolerability as assessed by the incidence of dose-limiting toxicities (DLTs)

Interventionalopen10 enrolledStarted 2023-07Completion 2025-061 site · United StatesWashington University School of Medicine