Vusolimogene oderparepvec
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Dosing in kidney impairment
When removing the needle, withdraw from the tumor slowly to avoid leakage of TUDRIQEV at the injection point. Figure 3: Radial Injection Administration in Deep or Visceral Tumor Note: Visceral organs may also include the lung, kidney or other organs. If necessary for injection, insert an introducer needle into the visceral organ where the tumor is to be treated as shown in Figure 4.
Pass the primed higher gauge TUDRIQEV needle through the introducer needle into the target tumor and inject TUDRIQEV slowly. Redirect the needles and repeat until the full TUDRIQEV dose is dispensed. When removing the needle, withdraw from the tumor slowly to avoid leakage of TUDRIQEV at the injection point. Figure 4: Coaxial Injection Administration in Visceral Tumor with Image Guidance Note: Visceral organs may also include the lung, kidney or other organs.
Dispose of all materials (e.g. syringe, gloves, cleaning materials) that may have come in contact with TUDRIQEV as biohazardous waste. Monitor patients post injection for procedure related reactions and for at least 2 to 4 hours in patients undergoing injections for liver, lung, or kidney tumors. Figure 1a Figure 1b Figure 2a Figure 2b Figure 3a Figure 3b Figure 4a Figure 4b
Preparation and administration
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Preparation and Handling Avoid accidental exposure to TUDRIQEV by wearing appropriate personal protective equipment (PPE). Observe standard precautions when preparing and administering TUDRIQEV [see Warnings and Precautions ]. Clean surfaces that may have come in contact with TUDRIQEV (including spills) with broad spectrum virucidal agent such as 70% isopropanol alcohol or 1% sodium hypochlorite.
Dispose of the used vials and all materials that may have come in contact with TUDRIQEV as biohazardous waste. TUDRIQEV should be prepared by a healthcare professional experienced in the use of anticancer therapy. Determine the volume required for injection [see Dosage and Administration ] . Thaw TUDRIQEV vials inside the original carton at room temperature [15°C to 25°C (59°F to 77°F)] or during refrigeration [2°C to 8°C (36° to 46°F)].
DO NOT refreeze TUDRIQEV after thawing [see How Supplied/Storage and Handling ] . Swirl gently, inspect vial. Particles may be visible [see Description ] . If settlement occurs, re-suspend by gently swirling. DO NOT shake. Using aseptic technique, withdraw the required TUDRIQEV dosage volume from the vial(s) into the syringe(s) to be used for administration.
Select needles gauged between 17G and 27G based on the location and characteristics of the tumors to be injected. A higher needle gauge will allow for a smaller puncture in tissue and will reduce leakage of TUDRIQEV along the needle tract. A lower needle gauge is needed for fibrotic or deeper lesions. Administer TUDRIQEV within 2 hours of syringe preparation [see How Supplied/Storage and Handling ] .
Administration DO NOT administer TUDRIQEV into brain or spinal cord tumors or scalp tumors with moderate to extensive bone erosion. Avoid tumors that encase, invade, or occlude major blood vessels, major nerve structures, or airways. Avoid direct injection into blood vessels. Pre-Injection Clean the skin areas where the needle will be inserted with an alcohol swab and let dry.
Treat the injection site with a topical or local anesthetic agent, if necessary. DO NOT inject anesthetic agent directly into the lesion. Inject anesthetic agent around the periphery of the lesion. Intratumor Injection into Nonulcerated Superficial Tumors Administer TUDRIQEV via direct intratumor injection into superficial tumors using visualization and palpation for guidance.
Injection techniques are shown in Figure 1 and Figure 2. Insert the needle from the periphery at a shallow angle (less than 45-degree) to the base of the tumor. Avoid areas of necrosis and target viable tumor tissue. Using a single insertion point, partially inject TUDRIQEV slowly. While keeping the needle inserted at a single insertion point, partially withdraw, and move the needle to different viable areas of the tumor as shown in Figure 1 and disperse TUDRIQEV as uniformly as possible throughout the tumor.
Continue until the full dose is dispensed. Multiple insertion sites may be needed, depending on the size of the tumor. When removing the needle, withdraw from the tumor slowly to avoid leakage of TUDRIQEV at the insertion point. Figure 1: Injection Administration for Nonulcerated Superficial Tumors Intratumor Injection into Ulcerated Superficial Tumors DO NOT inject TUDRIQEV through areas of ulceration and/or necrosis.
Insert the needle from the periphery at a shallow angle (less than 45-degree) to the base of the tumor. Using multiple insertion points (radial insertion) as shown in Figure 2, partially inject TUDRIQEV slowly. Disperse TUDRIQEV as uniformly as possible throughout the tumor. Continue until the full volume is dispensed. Withdraw from the tumor slowly to avoid leakage of TUDRIQEV at the insertion point.
Figure 2: Injection Administration for Ulcerated Cutaneous Tumors Intratumor Injection into Deep or Visceral Lesions Administer TUDRIQEV via direct intratumor injection into deep or visceral tumors guided by imaging technology. Consider the safest needle placement when selecting tumors for injection to avoid major vessels.
Select hepatic tumors that are at a safe distance from the main portal vein and common bile duct. Select lung tumors that are at a safe distance from any lobar or segmental pulmonary arteries or veins or lobar or segmental bronchi. DO NOT inject tumors in both the right and left lung lobes on the same day. Injection administration techniques in deep or visceral tumors are shown in Figure 3 (radial injection) and Figure 4 (coaxial injection).
Insert the needle into the tumor through a single insertion point to the distal end of the tumor. Multi-prong or multi-orifice needles may be used. Partially inject TUDRIQEV slowly while withdrawing the needle from the tumor. Redirect the needle as shown in Figure 3 and repeat steps until the full TUDRIQEV dose is dispensed.
When removing the needle, withdraw from the tumor slowly to avoid leakage of TUDRIQEV at the injection point. Figure 3: Radial Injection Administration in Deep or Visceral Tumor Note: Visceral organs may also include the lung, kidney or other organs. If necessary for injection, insert an introducer needle into the visceral organ where the tumor is to be treated as shown in Figure 4.
Pass the primed higher gauge TUDRIQEV needle through the introducer needle into the target tumor and inject TUDRIQEV slowly. Redirect the needles and repeat until the full TUDRIQEV dose is dispensed. When removing the needle, withdraw from the tumor slowly to avoid leakage of TUDRIQEV at the injection point. Figure 4: Coaxial Injection Administration in Visceral Tumor with Image Guidance Note: Visceral organs may also include the lung, kidney or other organs.
Post-Injection Swab the injection site(s) and surrounding area with alcohol. Change gloves and apply a sterile occlusive dressing at each injection site. Instruct patients to keep the injection site(s) covered for at least 48 hours. Clean surfaces that may have come in contact with TUDRIQEV (including spills) with broad spectrum virucidal agent such as 70% isopropanol or 1% sodium hypochlorite.
Dispose of all materials (e.g. syringe, gloves, cleaning materials) that may have come in contact with TUDRIQEV as biohazardous waste. Monitor patients post injection for procedure related reactions and for at least 2 to 4 hours in patients undergoing injections for liver, lung, or kidney tumors. Figure 1a Figure 1b Figure 2a Figure 2b Figure 3a Figure 3b Figure 4a Figure 4b
Drug interactions
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- Vusolimogene oderparepvec
Label text (2 paragraphs)
Antivirals: Antiviral medications may reduce the efficacy of TUDRIQEV. Delay TUDRIQEV administration for 72 hours after antivirals. ( 7.1 )
7.1 Effects of Antivirals Antiviral medications may reduce the efficacy of TUDRIQEV. Patients receiving systemic antiviral treatment for herpetic infection should delay TUDRIQEV treatment for 72 hours after completion of antiviral therapy.
Contraindications
None. None. ( 4 )
Safety data
Reported adverse events (FAERS)
Liver injury (LiverTox)
LiverTox has no chapter for vusolimogene oderparepvec. Check the label's hepatic warnings.
Pregnancy and lactation
Pregnancy
8.1 Pregnancy Risk Summary There are no available data with TUDRIQEV in pregnant women to inform a drug-associated risk. The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Clinical Considerations If the patient becomes pregnant during treatment with TUDRIQEV, the patient should be apprised that there may be potential hazards to the fetus and neonate.
Women of childbearing potential should be advised to use an effective method of contraception to prevent pregnancy during treatment with TUDRIQEV, and 90 days after the last dose of TUDRIQEV. Animal Data In an embryofetal development study in pregnant rats, TUDRIQEV was intravenously administered at 5x10 6 (5 million) PFU per kg once every three days during fetal organogenesis (gestational days 4 through 16) and was not associated with placental transfer of TUDRIQEV, adverse maternal findings, or treatment-related effects on embryo-fetal development.
For breastfeeding, also see LactMed (National Library of Medicine), which summarizes milk levels and infant effects.
Supply and cost
Drug shortage status
Recalls (last 24 months)
Therapeutic equivalence (Orange Book)
Price ladder
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