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Plerixafor

Myelodysplastic Syndrome

Explore 296 assets in Myelodysplastic Syndrome
Floatz Rating
B62/100
Confidence
Indicative
v0.2
Sponsor
Stanford University
Modality
Small molecule
Development Phase
Phase 2
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
55High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Reduced Intensity Allogeneic HCT in Advanced Hematologic Malignancies w/T-Cell Depleted Graft
Active Not Recruiting
MGTA-145 + Plerixafor in the Mobilization of HSCs for Allogeneic Transplant in Hematologic Malignancies
Terminated
A Safety and Tolerability Study of CDX-301 With or Without Plerixafor for Stem Cell Mobilization in Matched Related Allogeneic Donor/Recipient Sibling Transplant Pairs
Terminated
A Phase II Study Evaluating the Safety and Efficacy of Subcutaneous Plerixafor
Completed
T-Cell Replete Haploidentical Donor Hematopoietic Stem Cell Plus Natural Killer (NK) Cell Transplantation in Patients With Hematologic Malignancies Relapsed or Refractory Despite Previous Allogeneic Transplant
Terminated
A Trial to Establish the Feasibility of Combining Either the Tyrosine Kinase Inhibitor AC220,CXCR4 Inhibitor Plerixafor or HSP90 Inhibitor Ganetespib With Chemotherapy in Older Patients With Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome.
Completed
Plerixafor and Sargramostim (GM-CSF) for Mobilization of Allogeneic Sibling Donors
Completed
Plerixafor and Filgrastim For Mobilization of Donor Peripheral Blood Stem Cells Before A Donor Peripheral Blood Stem Cell Transplant in Treating Patients With Hematologic Malignancies
Terminated
A Pediatric Study of a Plerixafor Containing Regimen In Second Allogeneic Stem Cell Transplantation
Completed
Study Evaluating AMD3100 for Transplantation of Sibling Donor Stem Cells in Patients With Hematological Malignancies
Completed
Show 1 more trial
AMD3100 With Busulfan, Fludarabine and Thymoglobulin for Allogeneic Stem Cell Transplant for AML and MDS
Withdrawn

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
73High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Myelodysplastic Syndrome

AssetSponsorPhaseRating
Plerixafor (this asset)Stanford UniversityP2B · 62
CyclophosphamideSawa Ito, MDP4BB
NivestimCity of Hope Medical CenterP4BB
BusulfanumSawa Ito, MDP4BB
DaunomycinOHSU Knight Cancer InstituteP3BB
CytarabineThe First Affiliated Hospital of Soochow UniversityP4BB
FludarabineCity of Hope Medical CenterP4BB
IdarubicinOHSU Knight Cancer InstituteP4BB
SitagliptinIndiana UniversityP2BB

+42 more in the Myelodysplastic Syndrome cohort

Other indications for Plerixafor

IndicationSponsorPhaseRating
Fanconi AnemiaP2BB · 70
Hodgkins LymphomaP2BB · 70
Non-Hodgkin LymphomaP4BB · 69

Scientific Foundation

Strength of the underlying biology: target validation, tractability, modality fit, and how related mechanisms have fared.
NR

Planned for methodology v0.2.

Development Feasibility

How realistically the program can be executed, drawing on modality precedent, enrollment dynamics, and sponsor delivery.
NR

Planned for methodology v0.2.

Commercial Opportunity

Commercial prize: addressable population, unmet need, and the value case for the indication.
NR

Planned for methodology v0.2.

IP & Exclusivity

Exclusivity position, covering patent protection and freedom-to-operate runway.
NR

Planned for methodology v0.2.

Manufacturing & Supply

Manufacturing and supply readiness, driven by modality process and scale-up risk.
NR

Planned for methodology v0.2.

Related assets

Citation

Floatz Terminal. Plerixafor in Myelodysplastic Syndrome. Methodology v0.2.
Rated under v0.2 effective July 8, 2026. Last refreshed July 8, 2026.
Accessed July 14, 2026.
https://terminal.floatz.ai/assets/plerixafor-myelodysplastic-syndrome

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