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cyclophosphamide

Generic: CYCLOPHOSPHAMIDE·Brand: CYCLOPHOSPHAMIDE, CYTOXAN, CYTOXAN (LYOPHILIZED), FRINDOVYX, Frindovyx, LYOPHILIZED CYTOXAN, NEOSAR

cyclophosphamide: sourced relationships with 1 company · 365 clinical trials tracked · 1 FDA decision.

cyclophosphamide evidence translation

What we can confirm

1 FDA record · 365 tracked trials

What it means

Source-backed records connect cyclophosphamide to NEXS; that link alone does not prove the drug works.

What to watch

Watch active trials and any change in FDA or trial status.
BioSniper AIPage evidence connected

Prepared research question

How could cyclophosphamide → NEXS affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 15 study sponsors
Dated Pipeline Records (2)
CompanyDated record stage
NEXUS BIOPHARMA INC (NEXS)
Reported 2024-10-29 · Current development: unknownSource
Approved
NEXUS BIOPHARMA INC (NEXS)
Reported 2024-10-29 · Current development: unknownSource
Approved
Clinical Trial Registry Records (365)showing 10 most recent

A Phase 1 Study to Evaluate BAFFR-Targeting CAR T Cells for Patients With Relapsed or Refractory B-Cell Acute Lymphoblastic Leukemia

NCT07758673Registry updated 2026-08-11·Phase 1
Not yet recruiting

Primary endpoint: Incidence of adverse events

Interventionalopen16 targetStarted 2027-04Completion 2028-072 sites · United StatesCity of Hope Medical Center

A Phase 3, Randomized, Open-label, Multicenter Study to Compare the Efficacy and Safety of BMS-986353, CD19-targeted NEX-T CAR T Cells, Versus Standard of Care in Participants With Active Systemic Sclerosis (Breakfree-SSc)

NCT07335562Registry updated 2026-09-18·Phase 3
Not yet recruiting

Primary endpoint: The absolute change from baseline in Forced Vital Capacity (FVC) in mL

InterventionalRandomizedopen92 targetStarted 2027-02Completion 2030-1150 sites · Belgium, Canada, France, Germany…Juno Therapeutics, Inc., a Bristol-Myers Squibb Company

A Phase I Study of Single Agent Epcoritamab Followed by Epcoritamab Plus Pola-R-Mini-CHP for Elderly/Unfit Patients With Previously Untreated DLBCL

NCT07714421Registry updated 2026-07-20·Phase 1
Not yet recruiting

Primary endpoint: Progression free survival

Interventionalopen20 targetStarted 2026-12Completion 2031-101 site · United StatesJonsson Comprehensive Cancer Center

A Phase I Trial of Lymphodepletion Intensification With Low Dose Total Body Irradiation With Dose Expansion for Standard-of-Care Tisagenlecleucel in Patients With Large B-Cell Lymphoma

NCT07676877Registry updated 2026-10-09·Phase 1
Recruiting

Primary endpoint: Dose-limiting toxicities

Interventionalopen18 targetStarted 2026-12Completion 2027-121 site · United StatesNathan Denlinger

A Phase 3 Multicenter, Randomized, Open-Label Study Evaluating the Safety and Efficacy of Etentamig (ABBV-383) Compared to Daratumumab, Cyclophosphamide, Bortezomib, and Dexamethasone (Dara-CyBorD) in Subjects With Newly Diagnosed Amyloid Light Chain (AL) Amyloidosis

NCT07793422Registry updated 2026-08-28·Phase 3·ABBV
Not yet recruiting

Primary endpoint: Number of Participants With Adverse Events

InterventionalRandomizedopen370 targetStarted 2026-11Completion 2034-12AbbVie

A Phase II Randomized Study of Blinatumomab With or Without Revumenib for Patients With KMT2A-Translocation B-Cell Acute Lymphoblastic Leukemia (ALL)/ Acute Leukemia With Ambiguous Lineage (ALAL) With Persistent Measurable Residual Disease (MRD)

NCT07636564Registry updated 2026-06-09·Phase 2
Not yet recruiting

Primary endpoint: Dose limiting toxicities (Safety run-in: Cohort A)

InterventionalRandomizedopen90 targetStarted 2026-10Completion 2032-04SWOG Cancer Research Network

CD45RA-depleted CD19-CAR T Cell Consolidation After TCRαβ+/CD19 B Cell-depleted Haploidentical Hematopoietic Cell Transplantation for Relapsed/Refractory CD19+ ALL and Lymphoma

NCT07257419Registry updated 2026-08-28·Phase 1
Recruiting

Primary endpoint: To assess the safety of combining CD19-CAR(Mem) T cells after TCRαβ+/CD19 depleted haploidentical donor transplantation for pediatric patients with relapsed/refractory CD19+ B-cell malignancies.

Interventionalopen70 targetStarted 2026-10Completion 2035-121 site · United StatesSt. Jude Children's Research Hospital

A Randomized Study of Dexrazoxane or Liposomal Doxorubicin in Newly Diagnosed Diffuse Large B-cell Lymphoma at High Risk for Heart Failure Events: the CARDIOPROTECT Trial

NCT07654426Registry updated 2026-06-17·Phase 2
Not yet recruiting

Primary endpoint: Left Ventricular Ejection Fraction (LVEF)

InterventionalRandomizedquadruple60 targetStarted 2026-10Completion 2035-121 site · United StatesBeth Israel Deaconess Medical Center

A Multicenter, Phase 1, Safety and Tolerability Study of CC-97540 (BMS- 986353) in Anti-Aquaporin 4 Antibody Positive Neuromyelitis Optica Patients

NCT07573332Registry updated 2026-07-17·Phase 1
Not yet recruiting

Primary endpoint: To evaluate the safety and tolerability of CC-97540 (BMS-986353) in participants with anti-AQP4 antibody positive NMO as determined by the proportion of patients experiencing DLTs

Interventionalopen5 targetStarted 2026-09Completion 2031-081 site · United StatesUniversity of Texas Southwestern Medical Center

Haploidentical Donor Hematopoietic Cell Transplant for Sickle Cell Disease

NCT07616154Registry updated 2026-07-23·Phase 2
Recruiting

Primary endpoint: GVHD-free and rejection free survival (GRFS)

Interventionalopen45 targetStarted 2026-09Completion 2035-091 site · United StatesSt. Jude Children's Research Hospital
FDA Decisions1 records
Approval1 INDICATIONS AND USAGE Cyclophosphamide is an alkylating drug indicated for treatment of adults and pediatric patients with: Malignant Diseases: malignant lymphomas: Hodgkin's disease, lymphocytic lymphoma, mixed-cell type lymphoma, histiocytic lymphoma, Burkitt's lymphoma; multiple myeloma, leukemias, mycosis fungoides, neuroblastoma, adenocarcinoma of ovary, retinoblastoma, breast carcinoma. ( 1.1 ) 1.1 Malignant Diseases Cyclophosphamide Injection is indicated for the treatment of adult and (NEXS)FDA ↗
ANDA216783UNKNOWNStandardIntravenousSolution

Frequently asked questions

Which companies have sourced relationships with cyclophosphamide?

cyclophosphamide has dated SEC/FDA relationship records for NEXUS BIOPHARMA INC.

How many clinical trials involve cyclophosphamide?

BioSniper tracks 365 clinical trials involving cyclophosphamide.

What is cyclophosphamide's latest FDA decision?

The most recent tracked FDA decision for cyclophosphamide is Approval for 1 INDICATIONS AND USAGE Cyclophosphamide is an alkylating drug indicated for treatment of adults and pediatric patients with: Malignant Diseases: malignant lymphomas: Hodgkin's disease, lymphocytic lymphoma, mixed-cell type lymphoma, histiocytic lymphoma, Burkitt's lymphoma; multiple myeloma, leukemias, mycosis fungoides, neuroblastoma, adenocarcinoma of ovary, retinoblastoma, breast carcinoma. ( 1.1 ) 1.1 Malignant Diseases Cyclophosphamide Injection is indicated for the treatment of adult and , dated October 29, 2024.