Permanent J Code for ANKTIVA: J9028


Injection, nogapendekin alfa inbakicept-pmln, for intravesical use, 1 microgram

Effective January 1 2025, ANKTIVA's J Code: J9028 will be active for billing. If your system does not auto-update, please add the ANKTIVA coding information to your claims processing systems.



Designated an FDA Breakthrough Therapy for BCG-unresponsive non-muscle invasive bladder cancer carcinoma in situ (CIS), the novel immunotherapy ANKTIVA® activates key killer cells of the body’s natural immune system to attack the bladder cancer, leading to a long-duration of complete response that for some patients exceeds 47 months.1


Coding Information:

HCPCS Code

J9028

HCPCS Descriptor

Injection, nogapendekin alfa inbakicept-pmln, for intravesical use, 1 microgram

HCPCS Units per Package

400

10-Digit NDC Code

81481-803-01

11-Digit NDC Code

81481-0803-01

Package Description

Carton containing 400 mcg/0.4 mL, single-dose vial

WAC per Package

$35,800

WAC per HCPCS

$89.50

ImmunityBio would appreciate your partnership in updating systems and locations involved with ANKTIVA's billing and coding information.

Visit ANKTIVA.com

Indication and Important Safety Information


INDICATION AND USAGE: ANKTIVA is an interleukin-15 (IL-15) receptor agonist indicated with Bacillus Calmette-Guerin (BCG) for the treatment of adult patients with BCG-unresponsive non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ (CIS) with or without papillary tumors.


WARNINGS AND PRECAUTIONS: Risk of Metastatic Bladder Cancer with Delayed Cystectomy. Delaying cystectomy can lead to the development of muscle invasive or metastatic bladder cancer, which can be lethal. If patients with CIS do not have a complete response to treatment after a second induction course of ANKTIVA with BCG, reconsider cystectomy.


DOSAGE AND ADMINISTRATION: For lntravesical Use Only. Do not administer by subcutaneous or intravenous routes. Instill intravesically only after dilution. Total time from vial puncture to the completion of the intravesical instillation should not exceed 2 hours.


USE IN SPECIFIC POPULATIONS: Pregnancy: May cause fetal harm. Advise females of reproductive potential of the potential risk to a fetus and to use effective contraception.


ADVERSE REACTIONS: The most common (≥15%) adverse reactions, including laboratory test abnormalities, are increased creatinine, dysuria, hematuria, urinary frequency, micturition urgency, urinary tract infection, increased potassium, musculoskeletal pain, chills and pyrexia.


For more information about ANKTIVA, please see the Full Prescribing Information at www.anktiva.com.


You are encouraged to report negative side effects of prescription drugs to FDA. Visit www.FDA.gov/medwatch or call 1-800-332-1088. You may also contact lmmunityBio at 1-877-ANKTIVA (1-877-265-8482)

References:



  1. ANKTIVA Package insert. lmmunityBio, Inc., 2024; Represents the upper limit of the range of duration of response.

ANKTIVA is a registered trademark of ImmunityBio, Inc.

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