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Profile for Tradename: VANIQA

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Vaniqa is a drug marketed by Skinmedica and is included in one NDA. It is available from two suppliers. There is one patent protecting this drug.

The generic ingredient in VANIQA is eflornithine hydrochloride. There is one drug master file entry for this compound. Two suppliers are listed for this compound. Additional details are available on the eflornithine hydrochloride profile page.

Summary for Tradename: VANIQA

Patents:1
Applicants:1
NDAs:1
Suppliers: see list2

Pharmacology for Tradename: VANIQA

Clinical Trials for: VANIQA

Trial of Eflornithine Plus Sulindac in Patients With Familial Adenomatous Polyposis (FAP)
Status: Recruiting Condition: Familial Adenomatous Polyposis

A Trial of Low Dose Sulindac Combined With Eflornithine in Patients With Familial Adenomatous Polyposis (FAP)
Status: Withdrawn Condition: Familial Adenomatous Polyposis

Eflornithine To Prevent Cervical Cancer in Patients With Cervical Intraepithelial Neoplasia
Status: Completed Condition: Cervical Cancer; Precancerous Condition

Acetylsalicylic Acid and Eflornithine in Treating Patients at High Risk for Colorectal Cancer
Status: Recruiting Condition: Adenomatous Polyp

S0820, Adenoma and Second Primary Prevention Trial
Status: Recruiting Condition: Colorectal Neoplasms

Eflornithine and Sulindac in Preventing Colorectal Cancer in Patients With Colon Polyps
Status: Completed Condition: Precancerous Condition

Celecoxib With or Without Eflornithine in Preventing Colorectal Cancer in Patients With Familial Adenomatous Polyposis
Status: Completed Condition: Colorectal Cancer; Familial Adenomatous Polyposis

Eflornithine and/or Diclofenac in Treating Patients With Sun-Damaged Skin
Status: Completed Condition: Non-melanomatous Skin Cancer

Neoadjuvant Eflornithine and Bicalutamide Compared With Eflornithine Alone, Bicalutamide Alone, and No Neoadjuvant Therapy in Treating Patients With Localized Prostate Cancer Undergoing Brachytherapy or Radical Prostatectomy
Status: Completed Condition: Prostate Cancer

Clinical Study to Assess the Tolerability, Feasibility and Effectiveness of Nifurtimox and Eflornithine (NECT) for the Treatment of Trypanosoma Brucei Gambiense Human African Trypanosomiasis (HAT) in the Meningo-encephalitic Phase
Status: Completed Condition: Human African Trypanosomiasis

Courtesy of ClinicalTrials.org
See more clinical trials for this drug
Glossary
Applicant Tradename Generic Name Dosage NDA Approval Date Type RLD Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Skinmedica
VANIQA
eflornithine hydrochloride
CREAM;TOPICAL021145Jul 27, 2000RXYes5,648,394<disabled><disabled>
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