Cyclophosphamide

Acute Coryza, Retinoblastoma, Lymphoma, Large B-Cell, Diffuse + 20 more

Treatment

41 FDA approvals

20 Active Studies for Cyclophosphamide

What is Cyclophosphamide

Cyclophosphamide

The Generic name of this drug

Treatment Summary

Cyclophosphamide is a medication used to treat cancer, including lymphoma and leukemia. It must be processed in the liver to become an active form of chemotherapy. Side effects of the drug include hair loss, infertility, birth defects, and an increased risk of cancer. It is also used to shear sheep.

Cyclophosphamide

is the brand name

image of different drug pills on a surface

Cyclophosphamide Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

Cyclophosphamide

Cyclophosphamide

1959

75

Approved as Treatment by the FDA

Cyclophosphamide, otherwise called Cyclophosphamide, is approved by the FDA for 41 uses like Retinoblastoma and Lung Cancers .

Retinoblastoma

Lung Cancers

Glomerulonephritis

Non-Hodgkin's Lymphoma (NHL)

Adenocarcinoma of the Ovaries

Acute monocytic leukemia

histiocytic lymphoma

Hodgkins Disease (HD)

Acute Myeloid Leukemia (AML)

Breast Cancer

Multiple Myeloma (MM)

Disseminated Neuroblastoma

Nephrotic syndrome with lesion of minimal change glomerulonephritis

Chronic Myeloid Leukemia (CML)

Leukemia, Myelocytic, Acute

Burkitt Lymphoma (BL)

Lymphocytic Lymphomas

mixed-cell type lymphoma

Acute Lymphoblastic Leukemia (ALL)

Malignant Lymphomas

Chronic Lymphocytic Leukemia (CLL)

Hodgkin Disease

failure with corticosteroid therapy

Lung Cancer

Acute Myeloid Leukemia

Acute Coryza

Erythema Induratum

Neuroblastoma

Lymphoma, Non-Hodgkin

Acute Lymphoblastic Leukemia

Leukemia, Lymphocytic, Chronic, B-Cell

Leukemia, Myeloid, Acute

Breast Cancer

Non-Hodgkin's Lymphoma

Leukemia, Myelogenous, Chronic, BCR-ABL Positive

Lymphoma, Non-Hodgkin

Adenocarcinoma

Multiple Myeloma

Lymphoma, Large B-Cell, Diffuse

Chronic Lymphocytic Leukemia

Retinoblastoma

Effectiveness

How Cyclophosphamide Affects Patients

Cyclophosphamide is a type of medication used to treat cancer. It works by adding chemicals called alkyl groups to DNA, which prevents the cells from dividing and stops them from growing. It also adds methyl or other alkyl groups to molecules that should not be there, which disrupts how DNA works and causes the cells to die. Alkylating agents are cell cycle-nonspecific, meaning they affect any cell at any stage of its life cycle.

How Cyclophosphamide works in the body

Alkylating agents are drugs that prevent cancer cells from reproducing by damaging their DNA. They do this in three ways: by attaching alkyl molecules to the DNA, creating bonds between the atoms of the DNA, and causing the nucleotides to mispair. As a result of this damage, the DNA is unable to be copied, preventing further cancer cell growth.

When to interrupt dosage

The advised dosage of Cyclophosphamide is contingent upon the diagnosed condition, for example Lymphoma, Glomerulonephritis and Leukemia, Myelocytic, Acute. The measure of dosage varies depending on the administration technique (e.g. Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular or Powder, for solution - Intravenous) featured in the table below.

Condition

Dosage

Administration

Breast Cancer

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Leukemia, Lymphocytic, Chronic, B-Cell

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Hodgkin Disease

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Retinoblastoma

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Lymphoma, Large B-Cell, Diffuse

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Lymphoma, Non-Hodgkin

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Acute Myeloid Leukemia

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Acute Lymphoblastic Leukemia

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Lung Cancer

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

failure with corticosteroid therapy

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Leukemia, Myelogenous, Chronic, BCR-ABL Positive

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Lymphoma, Non-Hodgkin

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Chronic Lymphocytic Leukemia

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Multiple Sclerosis

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Erythema Induratum

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Glomerulonephritis

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Acute Coryza

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Lupus

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Leukemia, Myeloid, Acute

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Neuroblastoma

, 25.0 mg, 50.0 mg, 200.0 mg, 500.0 mg, 1000.0 mg, 2000.0 mg, 100.0 mg/mL, 20.0 mg/mL, 50.0 mg/mL, 200.0 mg/mL, 1000.0 mg/mL, 500.0 mg/mL

Oral, Tablet - Oral, Tablet, , Capsule, Capsule - Oral, Powder, for solution, Intravenous, Powder, for solution - Intravenous, Parenteral, Powder, for solution - Parenteral, Injection, powder, for solution - Intravenous; Oral, Injection, powder, for solution, Intravenous; Oral, Injection, powder, lyophilized, for solution, Injection, powder, lyophilized, for solution - Intravenous; Oral, Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, powder, for solution - Intramuscular; Intraperitoneal; Intrapleural; Intravascular, Injection, solution - Intravenous, Injection, solution, Injection, Concentrate, Concentrate - Intravenous, Injection - Intravenous

Warnings

Cyclophosphamide Contraindications

Condition

Risk Level

Notes

severely depressed bone marrow function

Do Not Combine

Urinary Bladder Neck Obstruction

Do Not Combine

There are 20 known major drug interactions with Cyclophosphamide.

Common Cyclophosphamide Drug Interactions

Drug Name

Risk Level

Description

2-Methoxyethanol

Major

The risk or severity of adverse effects can be increased when Cyclophosphamide is combined with 2-Methoxyethanol.

9-(N-methyl-L-isoleucine)-cyclosporin A

Major

The risk or severity of adverse effects can be increased when Cyclophosphamide is combined with 9-(N-methyl-L-isoleucine)-cyclosporin A.

Abemaciclib

Major

The metabolism of Abemaciclib can be increased when combined with Cyclophosphamide.

Abetimus

Major

The risk or severity of adverse effects can be increased when Cyclophosphamide is combined with Abetimus.

Acalabrutinib

Major

The metabolism of Acalabrutinib can be increased when combined with Cyclophosphamide.

Cyclophosphamide Toxicity & Overdose Risk

Common side effects of taking this drug include lowered white blood cell count, fever, hair loss, nausea, vomiting, and diarrhea.

image of a doctor in a lab doing drug, clinical research

Cyclophosphamide Novel Uses: Which Conditions Have a Clinical Trial Featuring Cyclophosphamide?

1165 active clinical trials are currently being conducted to examine the potential of Cyclophosphamide to treat Breast Cancer, Lymphocytic Lymphomas and Multiple Myeloma.

Condition

Clinical Trials

Trial Phases

Acute Myeloid Leukemia

267 Actively Recruiting

Phase 2, Phase 3, Phase 1, Phase 4, Not Applicable, Early Phase 1

Multiple Sclerosis

127 Actively Recruiting

Phase 3, Not Applicable, Phase 4, Phase 2, Phase 1, Early Phase 1

Non-Hodgkin's Lymphoma

115 Actively Recruiting

Phase 1, Phase 2, Not Applicable, Phase 3, Early Phase 1, Phase 4

Hodgkin Disease

3 Actively Recruiting

Not Applicable, Phase 1

Multiple Myeloma

6 Actively Recruiting

Phase 1, Phase 2

Lung Cancer

168 Actively Recruiting

Phase 1, Not Applicable, Phase 3, Phase 2, Early Phase 1

Lymphoma, Large B-Cell, Diffuse

0 Actively Recruiting

Chronic Lymphocytic Leukemia

142 Actively Recruiting

Phase 1, Phase 2, Not Applicable, Phase 3, Early Phase 1, Phase 4

Acute Lymphoblastic Leukemia

120 Actively Recruiting

Phase 1, Phase 2, Phase 3, Not Applicable, Early Phase 1, Phase 4

Adenocarcinoma

2 Actively Recruiting

Phase 2, Phase 1

Leukemia, Myelogenous, Chronic, BCR-ABL Positive

0 Actively Recruiting

Neuroblastoma

0 Actively Recruiting

Glomerulonephritis

1 Actively Recruiting

Phase 3

Leukemia, Myeloid, Acute

0 Actively Recruiting

Erythema Induratum

0 Actively Recruiting

failure with corticosteroid therapy

0 Actively Recruiting

Retinoblastoma

5 Actively Recruiting

Phase 2, Phase 1

Lymphoma, Non-Hodgkin

1 Actively Recruiting

Phase 1

Breast Cancer

21 Actively Recruiting

Phase 2, Phase 1, Not Applicable

Lupus

9 Actively Recruiting

Not Applicable, Phase 1, Phase 2, Early Phase 1

Cyclophosphamide Reviews: What are patients saying about Cyclophosphamide?

5

Patient Review

9/13/2010

Cyclophosphamide for Scleroderma Lung Disease

I've been on this medication for a short time, so it's hard to say if it's effective yet. I have noticed some hair loss and decreased appetite. When I do eat, I sometimes feel nauseous. It seems like my breathing is better, but the change has been very gradual.

4.7

Patient Review

3/15/2011

Cyclophosphamide for Cancer of the Ovary

This medicine has been incredibly effective, moreso than I could have hoped. My doctors decided to try something new on my 8th battle with cancer, and I'm so glad they did. As a college student, it's important to me that I can still go to school and work while taking this medication. The nausea has been tough to deal with but it's better than chemotherapy by far.

4.7

Patient Review

5/26/2008

Cyclophosphamide for Breast Cancer that has Spread to Another Part of the Body

4.3

Patient Review

9/1/2012

Cyclophosphamide for Scleroderma Lung Disease

I took this medication to get my Lupus under control, and it was successful. However, I experienced some troubling side effects afterwards that required me to take another medication. Thankfully, my liver returned to normal a few months later.

4

Patient Review

8/1/2008

Cyclophosphamide for Multiple Myeloma

3.7

Patient Review

10/13/2010

Cyclophosphamide for Malignant Tumor of the Kidney

I've been on this drug for over two years now and have had no significant side effects. My PFTs (not sure what this stands for) were stable when I switched to this medication, and I take 5mg of prednisone daily as well.

3.3

Patient Review

5/12/2009

Cyclophosphamide for Nephrotic Syndrome

I experienced few side effects with this drug, which is great compared to many other drugs I've tried. The only downside is that it didn't completely solve my hair loss issue, but it did help somewhat.

3

Patient Review

2/4/2014

Cyclophosphamide for Acute Monocytic Leukemia

I experienced a lot of abdominal pain, pelvic pain, cramps, burning, and watery stools while on this medication. I also had anal pressure and pain, gas, bloating, and a frequent urge to defecate. As a result of all these side effects, I lost weight and my appetite completely vanished. I have been off the medication for almost two months now and I still haven't had a normal stool.

3

Patient Review

7/23/2009

Cyclophosphamide for Scleroderma Lung Disease

My father had to be taken off this drug due to mental side effects. He was also taking dexamethasone, which may have contributed to the confusion and delusions he experienced.

2.7

Patient Review

10/26/2007

Cyclophosphamide for Breast Cancer that has Spread to Another Part of the Body

2.7

Patient Review

2/18/2009

Cyclophosphamide for Cancer of the Ovary

2

Patient Review

4/30/2012

Cyclophosphamide for Systemic Lupus Erythematosus

I started this medication after my OC recurred. So far, I'm liking it because I haven't experienced any hair loss or severe nausea.

1

Patient Review

1/14/2013

Cyclophosphamide for Cancer of the Ovary

I have now been on Cellcept twice, and can attest to its ineffectiveness. Not only does it lower your immunity to the point where you become susceptible to infection, but it also doesn't do anything to prevent the Scleroderma from coming back.

1

Patient Review

3/15/2009

Cyclophosphamide for Acute Monocytic Leukemia

I have recently been placed on this medication, but I haven't taken it for long enough to know if it's effective.
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Patient Q&A Section about cyclophosphamide

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is cyclophosphamide a chemo or immunotherapy?

"Cyclophosphamide is an alkylating chemotherapeutic agent that suppresses the immune system."

Answered by AI

What is the cyclophosphamide used for?

"Cyclophosphamide is a medication used to treat cancer in various parts of the body, including the ovaries, breast, blood and lymph system, nerves, and eyes. It is also used for treating multiple myeloma and skin tumors."

Answered by AI

Is cyclophosphamide a steroid?

"Cyclophosphamide is sometimes called a "steroid-sparing agent" because it has different side effects than prednisone."

Answered by AI

How cyclophosphamide is given?

"This medication can be administered in various ways depending on the diagnosis, including intravenously, orally in tablet form, or by injection into a muscle, the abdominal lining, or the lining of the lung."

Answered by AI

Clinical Trials for Cyclophosphamide

Image of Memoral Sloan Kettering at Basking Ridge (Limited Protocol Activities) in Basking Ridge, United States.

Ivosidenib + Azacitidine + Venetoclax for Acute Myeloid Leukemia

18+
All Sexes
Basking Ridge, NJ

The researchers are doing this study to find out whether a 3-drug combination of ivosidenib, azacitidine, and venetoclax followed by maintenance therapy with ivosidenib alone is an effective treatment approach for people with newly diagnosed acute myeloid leukemia (AML) that has an IDH mutation. Maintenance therapy is additional treatment given to help keep cancer from coming back after it has disappeared following the first course of treatment. The researchers will also look at the safety of the treatment approach and what kind of a time commitment it involves for participants.

Phase 2
Recruiting

Memoral Sloan Kettering at Basking Ridge (Limited Protocol Activities) (+6 Sites)

Kuo-Kai Chin, MD

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Image of Beth Israel Deaconess Medical Center in Boston, United States.

T-Cell Therapy + Vaccine + Drugs for Acute Myeloid Leukemia

Any Age
All Sexes
Boston, MA

The goal of this research study is to test if the combination of a new T cell therapy (dendritic cell (DC) / acute myeloid leukemia (AML) primed T cells), vaccine (DC/AML fusion vaccine) and standard of care decitabine and venetoclax is feasible and safe and effective for treatment of acute myeloid leukemia (AML). The names of the study drugs involved in this study are: * DC/AML fusion vaccine (immune cell vaccine) * Granulocyte-macrophage colony-stimulating factor (GM-CSF) (a type of growth factor or hormone) * DC/AML Primed T cells (immune cells) * Decitabine (a type of chemotherapy drug) * Venetoclax (a type of antineoplastic agent)

Phase 1
Waitlist Available

Beth Israel Deaconess Medical Center

David Avigan, MD

Image of University of Illinois at Chicago in Chicago, United States.

Functional Balance Intervention for Multiple Sclerosis

40 - 90
All Sexes
Chicago, IL

The study involves a two-arm, Phase 1, randomized controlled clinical trial designed to establish the feasibility and effects of a Functional Balance Intervention (FBI) on physical and cognitive function, as well as measures of daily living among persons with multiple sclerosis (PwMS). Combined Specific Aims: Aim 1: Examine the effect of the FBI (Intervention Group) on physical function in PwMS compared to a stretching program (Control Group). Hypothesis 1: After four months of training, the FBI group will show significantly greater improvements in physical function compared to the stretching group. Aim 2: Examine the effect of the multicomponent FBI on cognitive function in PwMS compared to the stretching program. Hypothesis 2: After four months of training, the FBI group will show significantly greater improvements in cognitive function compared to the stretching group. Aim 3: Examine the effects of the multicomponent FBI compared to the Control Group among PwMS on measures of daily living (dual-task performance, balance confidence, community mobility, and quality of life). Hypothesis 3: After four months of training, the FBI group will show significantly greater improvements in measures of daily living compared to the stretching group. All assessment sessions will be conducted virtually via Zoom. All measures collected during the initial screening, pre-training assessment, training progression, and mid- and post-training assessment sessions will be administered either via Zoom with a Helper Buddy present or through survey links sent to participants via the UIC REDCap system. The training sessions will be performed independently by the participants in the presence of a Helper Buddy. The investigators will recruit 75 people with multiple sclerosis (PwMS) for this study. Eligible participants will be randomized to either the FBI (Intervention) or stretching (Control) group, followed by an onboarding session with a designated Helper Buddy. Training will occur twice weekly for four months. Based on the anticipated attrition rate, the investigators aim for 40 PwMS to complete the post-training assessments and finish the study.

Recruiting
Has No Placebo

University of Illinois at Chicago

Image of HealthPartners Frauenshuh Cancer Research Center in Saint Louis Park, United States.

Axelopran for Cancer

18+
All Sexes
Saint Louis Park, MN

The primary objective of this single arm, open label, phase II trial is to determine if axelopran use impacts cancer control in patients with advanced cancers of the lung, breast, pancreas, and prostate. The primary study period for assessing the primary aim is through day 43 (6 weeks). The main questions it aims to answer are: * Does axelopran show a signal for efficacy in slowing tumor progression? * Is axelopran safe and tolerable for long-term use in this patient population? * Does axelopran show a signal for efficacy in improving bowel function and quality of life? * Does axelopran show a signal for efficacy in reducing systemic inflammation, cachexia, and prognostic serum biomarkers of inflammation? Patients will take axelopran as monotherapy after relapse or progression on or after standard systemic therapy. Clinician and patient must be willing to attempt a delay in next line of systemic cancer therapy (if available) until day 43 to assess change in cancer status on repeat imaging. Clinician can move to the next line of therapy whenever deemed clinically necessary. Participants will: * take oral axelopran capsules daily for up to 1 year, or longer if deriving benefit * attend 10 in-person study visits, each lasting approximately 1-2 hours * complete study procedures including but not limited to imaging exams, blood draws, electronic health surveys, and physical assessments

Phase 2
Waitlist Available

HealthPartners Frauenshuh Cancer Research Center (+1 Sites)

Dylan Zylla, MD, MS

Glycyx MOR Inc.

Have you considered Cyclophosphamide clinical trials?

We made a collection of clinical trials featuring Cyclophosphamide, we think they might fit your search criteria.
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Image of University of California Davis Comprehensive Cancer Center in Sacramento, United States.

Olutasidenib + Azacitidine for Acute Myeloid Leukemia

18+
All Sexes
Sacramento, CA

This phase II trial studies how well giving olutasidenib with azacitidine, followed by olutasidenib maintenance, works in treating patients with IDH1-mutated acute myeloid leukemia (AML) who have received prior treatment with venetoclax plus a hypomethylating agent (HMA-Ven). Olutasidenib and azacitidine may inhibit the growth of cancer cells by blocking certain enzymes required for cell growth. Maintenance therapy can help prevent or delay cancer from coming back. Olutasidenib with azacitidine followed by olutasidenib maintenance may be effective in treating patients with IDH1-mutated AML who have received prior HMA-Ven.

Phase 2
Recruiting

University of California Davis Comprehensive Cancer Center

Brian Jonas, MD

Image of University of Nebraska Medical Center in Omaha, United States.

Exercise for Blood Cancer Survivors

18+
All Sexes
Omaha, NE

Older survivors of blood cancer are at a high risk of accelerated biological aging, which increases their risk of developing multiple aging-related conditions. Whereas physical exercise can improve overall health, older cancer survivors do not meet the recommended physical activity, highlighting the need to develop behavioral interventions to increase adherence. Several other knowledge gaps exist to implement exercise interventions in older survivors of blood cancer; the dose and duration of exercise necessary to slow biological aging in older blood cancer survivors remain unknown. To bridge these gaps in knowledge, we have designed a Phase 2 randomized control trial to test the effects of behavioral and exercise interventions on various outcomes.

Phase 2
Waitlist Available

University of Nebraska Medical Center

Have you considered Cyclophosphamide clinical trials?

We made a collection of clinical trials featuring Cyclophosphamide, we think they might fit your search criteria.
Go to Trials