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Floatz Rating
B60/100
Confidence
Indicative
v0.2
Sponsor
Center for International Blood and Marrow Transplant Research
Modality
protein_peptide
Development Phase
Phase 3
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
57High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
A Platform Protocol to Investigate Post-Transplant Cyclophosphamide-Based Graft-Versus-Host Disease Prophylaxis in Patients With Hematologic Malignancies Undergoing Mismatched Unrelated Donor Peripheral Blood Stem Cell Transplantation
Recruiting
Panobinostat Combined With High-Dose Gemcitabine/Busulfan/Melphalan With Autologous Stem Cell Transplant for Patients With Refractory/Relapsed Lymphoma
Withdrawn
Lenalidomide Combined With Vorinostat/Gemcitabine/Busulfan/Melphalan With Autologous Stem-Cell Transplantation in Diffuse Large B-Cell Lymphoma of the ABC Subtype
Terminated
Vorinostat With Gemcitabine, Busulfan, and Melphalan With Stem Cell Transplant (SCT) in Relapsed or Refractory Lymphoid Malignancies
Completed
High-Dose Gemcitabine, Busulfan and Melphalan for Patients With Refactory Hodgkin's Disease
Completed
Palifermin After Haploidentical PBSCT
Withdrawn
Gemcitabine Plus Busulfan, Melphalan and Hematopoietic Cell Transplant for Advanced Lymphoid Malignancies
Completed
Palifermin for the Reduction of Oral Mucositis in Single-dose Evaluation (PROMISE)
Completed
Pharmacokinetic Study of Palifermin in Subjects Receiving Radiation Therapy and Chemotherapy Followed by Blood Stem Cell Support
Completed
Growth Factor to Prevent Oral Mucositis in Patients With Hematologic Cancer
Completed
Show 1 more trial
Biological Therapy in Treating Patients Undergoing Radiation Therapy, Chemotherapy, and Peripheral Stem Cell Transplantation for Hematologic Cancer
Completed

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
65High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Lymphoma

AssetSponsorPhaseRating
Palifermin (this asset)Center for International Blood and Marrow Transplant ResearchP3B · 60
VinblastineIntensity Therapeutics, Inc.P4BBB
PrednisoloneThe Lymphoma Academic Research OrganisationP4BBB
CyclophosphamideBeth Israel Deaconess Medical CenterP4BB
Vincristine SulfateInhye AhnP3BB
BleomycinShandong Provincial HospitalP4BB
MethotrexateUniversity of ChicagoP4BB
RituximabCity of Hope Medical CenterP4BB
IsocyclophosphamideShanghai General Hospital, Shanghai Jiao Tong University School of MedicineP3BB

+42 more in the Lymphoma cohort

Other indications for Palifermin

IndicationSponsorPhaseRating
MucositisP3BB · 64
Non-Hodgkin LymphomaP4B · 63
Plasma Cell MyelomaP4B · 61

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. Palifermin in Lymphoma. 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/palifermin-lymphoma

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