Label: PYLARIFY- piflufolastat f-18 injection
- NDC Code(s): 71258-022-01
- Packager: Progenics Pharmaceuticals, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated June 17, 2024
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HIGHLIGHTS OF PRESCRIBING INFORMATION
These highlights do not include all the information needed to use PYLARIFY® safely and effectively. See full prescribing information for PYLARIFY.
PYLARIFY® (piflufolastat F 18) injection, for intravenous use
Initial U.S. Approval: 2021INDICATIONS AND USAGE
PYLARIFY is a radioactive diagnostic agent indicated for positron emission tomography (PET) of prostate-specific membrane antigen (PSMA) positive lesions in men with prostate cancer:
- with suspected metastasis who are candidates for initial definitive therapy.
- with suspected recurrence based on elevated serum prostate-specific antigen (PSA) level. (1)
DOSAGE AND ADMINISTRATION
- Recommended dose is 333 MBq (9 mCi) with an acceptable range of 296 MBq to 370 MBq (8 mCi to 10 mCi), administered as a bolus intravenous injection. (2.2)
- Initiate imaging approximately 60 minutes after PYLARIFY administration. The patient should void immediately prior to initiation of imaging. Image acquisition should start from mid-thigh and proceed to the skull vertex. (2.3, 2.4)
- See full prescribing information for additional preparation, handling, administration, imaging, and radiation dosimetry information. (2)
DOSAGE FORMS AND STRENGTHS
Injection: clear, colorless solution in a multiple-dose vial containing 37 MBq/mL to 2,960 MBq/mL (1 mCi/mL to 80 mCi/mL) of piflufolastat F 18 at calibration date and time. (3)
CONTRAINDICATIONS
None. (4)
WARNINGS AND PRECAUTIONS
- Risk of Image Misinterpretation: PYLARIFY uptake can be seen in a variety of tumor types as well as in non-malignant processes and normal tissues. Image interpretation errors can occur with PYLARIFY imaging. (5.1)
- Hypersensitivity Reactions: Monitor patients for hypersensitivity reactions, particularly patients with a history of allergy to other drugs and foods. (5.2)
- Radiation Risk: Ensure safe drug handling to protect patients and health care workers from unintentional radiation exposure. (5.3)
ADVERSE REACTIONS
The most common reported adverse reactions are headache, dysgeusia, and fatigue. (6.1)
To report SUSPECTED ADVERSE REACTIONS, contact Progenics Pharmaceuticals, Inc. at 1-800-362-2668 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
See 17 for PATIENT COUNSELING INFORMATION.
Revised: 3/2023
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Table of Contents
FULL PRESCRIBING INFORMATION: CONTENTS*
1 INDICATIONS AND USAGE
2 DOSAGE AND ADMINISTRATION
2.1 Radiation Safety – Drug Handling
2.2 Recommended Dosage and Administration Instructions
2.3 Patient Preparation
2.4 Image Acquisition
2.5 Image Display and Interpretation
2.6 Radiation Dosimetry
3 DOSAGE FORMS AND STRENGTHS
4 CONTRAINDICATIONS
5 WARNINGS AND PRECAUTIONS
5.1 Risk of Image Misinterpretation
5.2 Hypersensitivity Reactions
5.3 Radiation Risks
6 ADVERSE REACTIONS
6.1 Clinical Trials Experience
7 DRUG INTERACTIONS
8 USE IN SPECIFIC POPULATIONS
8.1 Pregnancy
8.2 Lactation
8.4 Pediatric Use
8.5 Geriatric Use
10 OVERDOSAGE
11 DESCRIPTION
11.1 Chemical Characteristics
11.2 Physical Characteristics
11.3 External Radiation
12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action
12.2 Pharmacodynamics
12.3 Pharmacokinetics
13 NONCLINICAL TOXICOLOGY
13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility
14 CLINICAL STUDIES
16 HOW SUPPLIED/STORAGE AND HANDLING
16.1 How Supplied
16.2 Storage and Handling
17 PATIENT COUNSELING INFORMATION
- *
- Sections or subsections omitted from the full prescribing information are not listed.
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1 INDICATIONS AND USAGE
PYLARIFY is indicated for positron emission tomography (PET) of prostate-specific membrane antigen (PSMA) positive lesions in men with prostate cancer:
- with suspected metastasis who are candidates for initial definitive therapy.
- with suspected recurrence based on elevated serum prostate-specific antigen (PSA) level.
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2 DOSAGE AND ADMINISTRATION
2.1 Radiation Safety – Drug Handling
PYLARIFY is a radioactive drug. Only authorized persons qualified by training and experience should receive, use, and administer PYLARIFY. Handle PYLARIFY with appropriate safety measures to minimize radiation exposure during administration [see Warnings and Precautions (5.3)]. Use waterproof gloves and effective radiation shielding, including syringe shields, when preparing and handling PYLARIFY.
2.2 Recommended Dosage and Administration Instructions
Recommended Dose
The recommended amount of radioactivity to be administered for PET imaging is 333 MBq (9 mCi) with an acceptable range of 296 MBq to 370 MBq (8 mCi to 10 mCi) administered as a single bolus intravenous injection.
Preparation and Administration
- Use aseptic technique and radiation shielding when preparing and administering PYLARIFY.
- Visually inspect the radiopharmaceutical solution. Do not use if it contains particulate matter or if it is discolored (PYLARIFY is a clear, colorless solution).
- Calculate the necessary volume to administer based on calibration time and required dose. PYLARIFY may be diluted with 0.9% Sodium Chloride Injection, USP.
- Assay the dose in a suitable dose calibrator prior to administration.
2.3 Patient Preparation
Instruct patients to drink water to ensure adequate hydration prior to administration of PYLARIFY and to continue drinking and voiding frequently for the first few hours following administration to reduce radiation exposure [see Warnings and Precautions (5.3)].
2.4 Image Acquisition
The recommended start time for image acquisition is 60 minutes after PYLARIFY injection. Starting image acquisition more than 90 minutes after injection may adversely impact imaging performance. Patients should void immediately prior to image acquisition. Position the patient supine with arms above the head. Image acquisition should start from mid-thigh and proceed to the skull vertex. Scan duration is 12 minutes to 40 minutes depending on the number of bed positions (typically 6 to 8) and acquisition time per bed position (typically 2 minutes to 5 minutes).
2.5 Image Display and Interpretation
PYLARIFY binds to prostate-specific membrane antigen (PSMA). Based on the intensity of the signals, PET images obtained using PYLARIFY indicate the presence of PSMA in tissues. Lesions should be considered suspicious if uptake is greater than physiologic uptake in that tissue or greater than adjacent background if no physiologic uptake is expected. Tumors that do not express PSMA will not be visualized. Increased uptake in tumors is not specific for prostate cancer [see Warnings and Precautions (5.1)].
2.6 Radiation Dosimetry
Radiation absorbed dose estimates are shown in Table 1 for organs and tissues of adult male patients from intravenous administration of PYLARIFY. The radiation effective dose resulting from administration of 370 MBq (10 mCi) of PYLARIFY to an adult weighing 70 kg is estimated to be 4.3 mSv. The radiation doses for this administered dose to the critical organs, which are the kidneys, liver, and spleen, are 45.5 mGy, 13.7 mGy, and 10 mGy respectively. When PET/CT is performed, exposure to radiation will increase by an amount dependent on the settings used in the CT acquisition.
Table 1. Estimated Radiation Absorbed Doses in Organs/Tissues in Adults who Received PYLARIFY Organ/Tissue Mean Absorbed dose per Unit Administered Activity
(mGy/MBq)Mean Standard Deviation Adrenal glands 0.0131 0.0013 Brain 0.0021 0.0003 Breasts 0.0058 0.0007 Gallbladder wall 0.0141 0.0012 Lower large intestine wall 0.0073 0.001 Small intestine 0.0089 0.0009 Stomach wall 0.0092 0.0008 Upper large intestine wall 0.0091 0.0009 Heart wall 0.0171 0.0022 Kidneys 0.123 0.0434 Liver 0.037 0.0058 Lungs 0.0102 0.0016 Muscle 0.0069 0.0008 Pancreas 0.0124 0.0011 Red bone marrow 0.0071 0.0007 Osteogenic cells 0.0099 0.0012 Skin 0.0052 0.0006 Spleen 0.0271 0.0115 Testes 0.0059 0.0008 Thymus gland 0.007 0.0008 Thyroid 0.0062 0.0009 Urinary bladder wall 0.0072 0.001 Effective dose 0.0116 (mSv/MBq) 0.0022 (mSv/MBq) - 3 DOSAGE FORMS AND STRENGTHS
- 4 CONTRAINDICATIONS
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5 WARNINGS AND PRECAUTIONS
5.1 Risk of Image Misinterpretation
Imaging interpretation errors can occur with PYLARIFY imaging. A negative image does not rule out the presence of prostate cancer and a positive image does not confirm the presence of prostate cancer. The performance of PYLARIFY for imaging of patients with biochemical evidence of recurrence of prostate cancer seems to be affected by serum PSA levels [see Clinical Studies (14)]. The performance of PYLARIFY for imaging of metastatic pelvic lymph nodes prior to initial definitive therapy seems to be affected by risk factors such as Gleason score and tumor stage [see Clinical Studies (14)]. PYLARIFY uptake is not specific for prostate cancer and may occur with other types of cancer as well as non-malignant processes and in normal tissues. Clinical correlation, which may include histopathological evaluation of the suspected prostate cancer site, is recommended.
5.2 Hypersensitivity Reactions
Monitor patients for hypersensitivity reactions, particularly patients with a history of allergy to other drugs and foods. Reactions may not be immediate. Always have trained staff and resuscitation equipment available.
5.3 Radiation Risks
Diagnostic radiopharmaceuticals, including PYLARIFY, expose patients to radiation [see Dosage and Administration (2.6)]. Radiation exposure is associated with a dose-dependent increased risk of cancer. Ensure safe handling and preparation procedures to protect patients and health care workers from unintentional radiation exposure. Advise patients to hydrate before and after administration and to void frequently after administration [see Dosage and Administration (2.3)].
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6 ADVERSE REACTIONS
6.1 Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
The safety of PYLARIFY was evaluated in 593 patients, each receiving one dose of PYLARIFY. The average injected activity was 340 ± 26 MBq (9.2 ± 0.7 mCi).
The adverse reactions reported in >0.5% of patients within the studies are shown in Table 2. In addition, a hypersensitivity reaction was reported in one patient (0.2%) with a history of allergic reaction.
Table 2. Adverse Reactions with a Frequency >0.5% in Patients Who Received PYLARIFY (n = 593) Adverse Reaction n (%) Headache 13 (2%) Dysgeusia 10 (2%) Fatigue 7 (1%) -
7 DRUG INTERACTIONS
Androgen deprivation therapy and other therapies targeting the androgen pathway
Androgen deprivation therapy (ADT) and other therapies targeting the androgen pathway, such as androgen receptor antagonists, may result in changes in uptake of PYLARIFY in prostate cancer. The effect of these therapies on performance of PYLARIFY PET has not been established.
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8 USE IN SPECIFIC POPULATIONS
8.1 Pregnancy
Risk Summary
PYLARIFY is not indicated for use in females. There is no information on the risk of adverse developmental outcomes in pregnant women or animals with the use of piflufolastat F 18. All radiopharmaceuticals, including PYLARIFY, have the potential to cause fetal harm depending on the fetal stage of development and the magnitude of the radiation dose.
8.4 Pediatric Use
The safety and effectiveness of PYLARIFY in pediatric patients have not been established.
8.5 Geriatric Use
Of the 593 patients in completed clinical studies of PYLARIFY, 355 (60%) were ≥65 years old, while 76 (12.8%) were ≥75 years old. The efficacy and safety of PYLARIFY appear similar in adult and geriatric patients with prostate cancer, although the number of patients in the trials was not large enough to allow definitive comparison.
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10 OVERDOSAGE
In the event of an overdose of PYLARIFY, reduce the radiation absorbed dose to the patient where possible by increasing the elimination of the drug from the body using hydration and frequent bladder voiding. A diuretic might also be considered. If possible, an estimate of the radiation effective dose administered to the patient should be made.
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11 DESCRIPTION
11.1 Chemical Characteristics
PYLARIFY contains fluorine 18 (F 18), radiolabeled prostate-specific membrane antigen inhibitor imaging agent. Chemically piflufolastat F 18 is 2-(3-{1-carboxy-5-[(6-[18F]fluoro-pyridine-3-carbonyl)-amino]-pentyl}ureido)-pentanedioic acid. The molecular weight is 441.4 and the structural formula is:
The chiral purity of the unlabeled piflufolastat F 18 precursor is greater than 99% (S,S).
PYLARIFY is a sterile, non-pyrogenic, clear, colorless solution for intravenous injection. Each milliliter contains 37 to 2,960 MBq (1 to 80 mCi) piflufolastat F 18 with ≤0.01 µg/mCi of piflufolastat at calibration time and date, and ≤ 78.9 mg ethanol in 0.9% sodium chloride injection USP. The pH of the solution is 4.5 to 7.0.
PYLARIFY has a radiochemical purity of at least 95% up to 10 hours following end of synthesis, and specific activity of at least 1000 mCi/µmol at the time of administration.
11.2 Physical Characteristics
PYLARIFY is radiolabeled with fluorine 18 (F 18), a cyclotron produced radionuclide that decays by positron emission to stable oxygen 18 with a half-life of 109.8 minutes. The principal photons useful for diagnostic imaging are the coincident pair of 511 keV gamma photons, resulting from the interaction of the emitted positron with an electron (Table 3).
Table 3. Principal Radiation Produced from Decay of Fluorine 18 Radiation Energy (keV) Abundance (%) Positron 249.8 96.9 Gamma 511 193.5 11.3 External Radiation
The point source air-kerma coefficient for F 18 is 3.75 × 10-17 Gy m2/(Bq s). The first half-value thickness of lead (Pb) for F 18 gamma rays is approximately 6 mm. The relative reduction of radiation emitted by F 18 that results from various thicknesses of lead shielding is shown in Table 4. The use of 8 cm Pb decreases the radiation transmission (i.e. exposure) by a factor of about 10,000.
Table 4. Radiation Attenuation of 511 keV Gamma Rays by Lead Shielding Shield Thickness cm of Lead (Pb) Coefficient of Attenuation 0.6 0.5 2 0.1 4 0.01 6 0.001 8 0.0001 -
12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action
Piflufolastat F 18 binds to cells that express PSMA, including malignant prostate cancer cells, which usually overexpress PSMA. Fluorine-18 (F 18) is a β+ emitting radionuclide that enables positron emission tomography.
12.2 Pharmacodynamics
The relationship between piflufolastat F 18 plasma concentrations and image interpretation has not been studied.
12.3 Pharmacokinetics
Distribution
Following intravenous administration of piflufolastat F 18, blood levels decline in a biphasic fashion. The distribution half-life is 0.17 ± 0.044 hours and the elimination half-life is 3.47 ± 0.49 hours.
Piflufolastat F 18 distributes to the kidneys (16.5% of administered activity), liver (9.3%), and lung (2.9%), within 60 minutes of intravenous administration.
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13 NONCLINICAL TOXICOLOGY
13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility
Animal studies to assess the carcinogenicity or mutagenic potential of piflufolastat have not been conducted. However, piflufolastat has the potential to be mutagenic because of the F 18 radioisotope.
No animal studies with piflufolastat have been performed to evaluate the potential impairment of fertility in males or females.
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14 CLINICAL STUDIES
The safety and efficacy of PYLARIFY were evaluated in two prospective, open-label, multi-center clinical studies in men with prostate cancer: OSPREY (NCT02981368) and CONDOR (NCT03739684).
OSPREY
OSPREY enrolled a cohort of 268 men with biopsy-proven prostate cancer who were considered candidates for radical prostatectomy and pelvic lymph node dissection. These patients were all considered to have high risk disease based on criteria such as Gleason score, PSA level, and tumor stage. Each patient received a single PYLARIFY PET/CT from mid-thigh to skull vertex.
Three central readers independently interpreted each PET scan for the presence of abnormal PYLARIFY uptake in pelvic lymph nodes in multiple subregions, including the common iliac lymph nodes. The readers were blinded to all clinical information. While readers also recorded the presence of PYLARIFY PET-positive lesions in the prostate gland and outside the pelvis, those results were not included in the primary efficacy analysis.
A total of 252 patients (94%) underwent standard-of-care prostatectomy and template pelvic lymph node dissection and had sufficient histopathology data for evaluation of the pelvic lymph nodes. Surgical specimens were separated into three regions: left hemipelvis, right hemipelvis, and other. For each patient, PYLARIFY PET results and histopathology results obtained from dissected pelvic lymph nodes were compared by surgical region. PET results in locations that were not dissected were excluded from analysis.
For the 252 evaluable patients, the mean age was 64 years (range 46 to 84 years), and 87% were white. The median serum PSA was 9.3 ng/mL. The total Gleason score was 7 for 19%, 8 for 46%, and 9 for 34% of the patients, with the remainder of the patients having Gleason scores of 6 or 10.
Table 5 shows PYLARIFY PET performance by reader through comparison to pelvic lymph node histopathology at the patient-level with region matching, such that at least one true positive region defines a true positive patient. Approximately 24% of the evaluable patients had pelvic lymph node metastases based on histopathology (95% confidence interval: 19%, 29%).
Table 5: Patient-Level, Region-Matched Performance of PYLARIFY PET for Detection of Pelvic Lymph Node Metastasis in OSPREY (n=252) Reader 1 Reader 2 Reader 3 Abbreviations: CI = confidence interval, PPV = positive predictive value, NPV = negative predictive value True Positive 23 17 23 False Positive 7 4 9 False Negative 36 43 37 True Negative 186 188 183 Sensitivity, % (95% CI) 39 (27, 51) 28 (17, 40) 38 (26, 51) Specificity, % (95% CI) 96 (94, 99) 98 (95, 99) 95 (92, 98) PPV, % (95% CI) 77 (62, 92) 81 (59, 93) 72 (56, 87) NPV, % (95% CI) 84 (79, 89) 81 (76, 86) 83 (78, 88) In exploratory analyses, there were numerical trends towards more true positive results among patients with total Gleason score of 8 or higher and among patients with tumor stage of T2c or higher relative to those patients with lower Gleason score or tumor stage.
CONDOR
CONDOR enrolled 208 patients with biochemical evidence of recurrent prostate cancer, defined by serum PSA of at least 0.2 ng/mL after radical prostatectomy (with confirmatory PSA level also at least
0.2 ng/mL) or by an increase in serum PSA of at least 2 ng/mL above the nadir after other therapies. The mean age was 68 years (range 43 to 91 years), and 90% of patients were white. The median serum PSA was 0.82 ng/mL. Prior treatment included radical prostatectomy in 85% of the patients.
All enrolled patients had conventional imaging evaluation (for most patients, CT or MRI) within 60 days prior to receiving PYLARIFY PET, and this evaluation was negative or equivocal for prostate cancer. All patients received a single PYLARIFY PET/CT from mid-thigh to skull vertex with optional imaging of the lower extremities.
Three central readers independently evaluated each PYLARIFY PET scan for the presence and location of positive lesions. Location of each lesion was categorized in one of 19 subregions that were grouped into 5 regions (prostate/prostate bed, pelvic lymph nodes, other lymph nodes, soft tissue, bone). The readers were blinded to all clinical information.
Depending on the reader, a total of 123 to 137 patients (59% to 66%) had at least one lesion that was identified as PYLARIFY PET-positive (Table 6, TP + FP + PET-Positive Without Reference Standard). The region most commonly observed to have a PYLARIFY PET-positive finding was pelvic lymph nodes (40% to 42% of all PET-positive regions) and the least common region was soft tissue (6% to 7%).
Depending on the reader, 99 to 104 patients with a PYLARIFY PET-positive region had location-matched composite reference standard information available (Evaluable Set, Table 6, TP + FP) that consisted of histopathology, imaging (CT, MRI, ultrasound, fluciclovine PET, choline PET, or bone scan) obtained within 60 days of the PYLARIFY PET scan, or response of serum PSA level to targeted radiotherapy. Reference standard information for PET-negative regions was not systematically collected in this study.
Table 6 shows patient-level performance results of PYLARIFY PET by reader, including location -matched positive predictive value [true positive / (true positive + false positive)], also known as Correct Localization Rate (CLR). For these results, a patient was considered true positive if they had at least one matching location positive on both PYLARIFY PET and the composite reference standard. In addition to calculating location-matched positive predictive value in the Evaluable Set (CLR), an exploratory analysis of positive predictive value in all scanned patients (Imputed CLR) was performed in which PYLARIFY PET-positive patients who lacked reference standard information were imputed using an estimated likelihood that at least one PET-positive lesion was reference standard positive, based on patient-specific factors.
Table 6: Patient-Level Performance of PYLARIFY PET in CONDOR (n=208) Reader 1 Reader 2 Reader 3 Abbreviations: TP = true positive, FP = false positive, CLR = location-matched positive predictive value in the Evaluable Set [TP/(TP + FP)], Imputed CLR = location-matched positive predictive value in all scanned patients using an imputation approach based on patient-specific factors for PET-Positive Without Reference Standard, CI = confidence interval True Positive (TP) 89 87 84 False Positive (FP) 15 13 15 PET-Positive Without Reference Standard 33 24 24 PET-Negative 71 84 85 CLR % (95% CI) 86 (79, 92) 87 (80, 94) 85 (78, 92) Imputed CLR % (95% CI) 78 (71, 85) 81 (74, 88) 79 (72, 86) An exploratory analysis of region-level positive predictive value using only PET-positive regions that had sufficient composite reference standard information to determine true positive or false positive status demonstrated results of 67% to 70% with the lower bound of the 95% confidence interval ranging from 59% to 63%.
The percentage of patients categorized as true positive in a location-matched analysis out of all patients scanned with PYLARIFY was an additional exploratory endpoint. Using the same imputation approach for PET-positive patients who lacked reference standard information as in Table 6 above, this value was 47% to 51%, with the lower bound of the 95% confidence interval ranging from 40% to 45%.
Table 7 shows patient-level PYLARIFY PET results from the majority read stratified by serum PSA level. Percent PET positivity was calculated as the proportion of patients with a positive PYLARIFY PET out of all patients scanned. Percent PET positivity includes patients determined to be either true positive or false positive as well as those in whom such determination was not made due to lack of composite reference standard information. The likelihood of a patient having at least one PYLARIFY PET-positive lesion generally increased with higher serum PSA level.
Table 7: Patient-Level PYLARIFY PET Results and Percent PET Positivity* Stratified by Serum PSA Level in the CONDOR Study Using Majority Result Among Three Readers (n=199)† PSA (ng/mL) PET positive patients PET negative patients Percent PET positivity, (95% CI) Total TP FP Without reference standard With reference standard Abbreviations: TP = true positive, FP = false positive, CI = confidence interval - *
- Percent PET positivity = PET positive patients/total patients scanned. PET positive patients include true positive and false positive patients as well as those who did not have reference standard information.
- †
- Six patients were excluded from this table due to lack of baseline PSA level. Three patients were excluded from this table due to lack of majority result among the categories true positive, false positive, PET positive without reference standard, and PET negative.
<0.5 24 11 4 9 45 35 (24, 46) 15 ≥0.5 and <1 18 12 3 3 18 50 (34, 66) 15 ≥1 and <2 21 15 3 3 10 68 (51, 84) 18 ≥2 57 50 3 4 6 90 (83, 98) 53 Total 120 88 13 19 79 60 (54, 67) 101 -
16 HOW SUPPLIED/STORAGE AND HANDLING
16.1 How Supplied
PYLARIFY injection is supplied in a 50 mL multiple-dose glass vial (NDC# 71258-022-01) containing a clear, colorless solution at a strength of 37 MBq/mL to 2,960 MBq/mL (1 mCi/mL to 80 mCi/mL) piflufolastat F 18 at calibration time and date.
16.2 Storage and Handling
Storage
Store PYLARIFY at controlled room temperature (USP) 20°C to 25°C (68°F to 77°F). PYLARIFY does not contain a preservative. Store PYLARIFY in the original container with radiation shielding. The expiration date and time are provided on the container label. Use PYLARIFY within 10 hours from the time of end of synthesis.
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17 PATIENT COUNSELING INFORMATION
Adequate Hydration
Instruct patients to drink a sufficient amount of water to ensure adequate hydration before their PET study and urge them to drink and urinate as often as possible during the first hours following the administration of PYLARIFY, in order to reduce radiation exposure [see Dosage and Administration (2.3) and Warnings and Precautions (5.3)].
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 80 mCi/mL Vial Label
Sterile
PYLARIFY®
(piflufolastat F 18) injectionNon-pyrogenic
37 MBq/mL to 2,960 MBq/mL (1 mCi/mL to 80 mCi/mL)
at end of synthesis (EOS)
Diagnostic – For Intravenous Use Only
Expires within 10 hours from EOSBatch #: _________
EOS Date:_________EOS Time: _________
Activity @ EOS:_________mCi
Concentration:_________mCi/mL
Volume:_________mL
Exp. Date:_________Exp. Time: _________
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INGREDIENTS AND APPEARANCE
PYLARIFY
piflufolastat f-18 injectionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71258-022 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PIFLUFOLASTAT F-18 (UNII: 3934EF02T7) (PIFLUFOLASTAT F-18 - UNII:3934EF02T7) PIFLUFOLASTAT F-18 80 mCi in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ISOTONIC SODIUM CHLORIDE SOLUTION (UNII: VR5Y7PDT5W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71258-022-01 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product 05/26/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA214793 05/26/2021 Labeler - Progenics Pharmaceuticals, Inc. (195551247) Establishment Name Address ID/FEI Business Operations Asymchem Life Science (Tianjin) Co., Ltd. 528176699 API MANUFACTURE(71258-022) Establishment Name Address ID/FEI Business Operations PETNET SOLUTIONS, INC. 134146484 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations SOFIE Co. dba SOFIE 079854636 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 026659644 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations N-Molecular Inc. dba SOFIE 079932600 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 961682551 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 961592982 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 101387665 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 965557486 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 603833208 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations SOFIE Co. dba SOFIE 032324142 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations SOFIE Co. dba SOFIE 928455851 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 128523862 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 033883716 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 103781071 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations N-Molecular, Inc. dba SOFIE 079932640 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations SOFIE Co. dba SOFIE 118258354 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 961593337 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations SOFIE Co. dba SOFIE 025600556 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations SOFIE Co. dba SOFIE 829109441 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations Precision Nuclear, LLC 879283633 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations SOFIE Co. dba SOFIE 078623800 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations SOFIE Co. dba SOFIE 832599976 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 117843428 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PETNET Solutions, Inc. 123562576 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations N-Molecular, Inc. dba SOFIE 079932634 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations PharmaLogic Colorado, LLC 117608150 POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION(71258-022) Establishment Name Address ID/FEI Business Operations The University of Utah DBA Cyclotron Radiochemistry Lab Huntsman 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