Peringatan Keamanan

There are no data regarding the effects of overdosage with piflufolastat F18. In the event of overdose, the amount of absorbed radiation can be mitigated by administered fluids and encouraging frequent bladder voiding. The use of diuretics to encourage voiding may also be considered.L34294

Piflufolastat F 18

DB14805

small molecule approved investigational

Deskripsi

Prostate cancer is the most common non-cutaneous malignancy affecting men in North AmericaA235344 - despite this, an ongoing challenge in prostate cancer therapy is the difficulty in imaging the extent and location of tumor metastases and recurrences.L34319 The images generated by positron emission tomography (PET) are less detailed than those obtained via MRI or CT, but are more sensitive and can reveal cancerous tissue in any area of the body provided the tissue is expressing the appropriate target protein. Prostate-specific membrane antigen (PSMA) is a transmembrane glycoprotein expressed in many tissues that plays a role in folate uptake and neurotransmitter release - it is expressed in the prostate at levels roughly 1000-fold greater than elsewhere in the body, and even higher in prostate cancer tissue.A235169 As such, it has become a desirable target for PET imaging of prostate cancer tissues.

Piflufolastat F18, also called F-18-DCFPyL, is a urea-based radiopharmaceutical that binds to PSMA and allows for the visualization of cancerous prostate tissue. It was first approved by the FDA in May 2021 under the brand name Pylarify and aims to allow for earlier and more accurate detection of suspected prostate cancer metastases or recurrences.L34324 On July 28, 2023, the EMA also approves Piflufolastat F18 under the brand name PYLCLARI for primary staging or localizing recurrence of prostate cancer.L47586

Struktur Molekul 2D

Berat 441.403
Wujud liquid

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) The half-life of distribution of piflufolastat F18 is 0.17 ± 0.044 hours and its elimination half-life is 3.47 ± 0.49 hours.[L34294]
Volume Distribusi 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.[L34294]
Klirens (Clearance) -

Absorpsi

Data absorpsi tidak tersedia.

Metabolisme

Data metabolisme tidak tersedia.

Rute Eliminasi

Piflufolastat F18 is eliminated via urinary excretion - within 8 hours of intravenous administration, approximately 50% of an administered dose is excreted in the urine.L34294

Interaksi Obat

10 Data
Flutamide Flutamide may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Nilutamide Nilutamide may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Bicalutamide Bicalutamide may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Cyproterone acetate Cyproterone acetate may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Enzalutamide Enzalutamide may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Relugolix Relugolix may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Apalutamide Apalutamide may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Darolutamide Darolutamide may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Chlormadinone Chlormadinone may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.
Chlormadinone acetate Chlormadinone acetate may decrease effectiveness of Piflufolastat F 18 as a diagnostic agent.

Target Protein

Glutamate carboxypeptidase 2 FOLH1

Referensi & Sumber

Synthesis reference: Shan L: 2-(3-{1-Carboxy-5-(6-[(18)Ffluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)-p entanedioic acid. PubMed:23256224

Contoh Produk & Brand

Produk: 3 • International brands: 1
Produk
  • Pylarify
    Injection • 80 mCi/1mL • Intravenous • US • Approved
  • Pylclari
    Injection, solution • 1000 MBq/mL • Intravenous • EU • Approved
  • Pylclari
    Injection, solution • 1500 MBq/mL • Intravenous • EU • Approved
International Brands
  • Pylarify — Lantheus Holdings, Inc.

Sekuens Gen/Protein (FASTA)

Sekuens dimuat saat dibutuhkan agar halaman tetap ringan.
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