{"id":308,"date":"2026-04-11T17:15:24","date_gmt":"2026-04-11T17:15:24","guid":{"rendered":"https:\/\/luciuspharmacy.com\/?post_type=product&#038;p=308"},"modified":"2026-09-30T09:05:13","modified_gmt":"2026-09-30T09:05:13","slug":"luciolap-olaparib-150-mgx120-tablets","status":"publish","type":"product","link":"https:\/\/luciuspharmacy.com\/ar\/product\/luciolap-olaparib-150-mgx120-tablets\/","title":{"rendered":"LuciOlap"},"content":{"rendered":"<p style=\"line-height:20px\"><span style=\";color:#3f3f3f;font-size:18px\"><strong style=\"\">HIGHLIGHTS OF PRESCRIBING INFORMATION <\/strong><\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"color:#3f3f3f;font-size:18px\"><strong style=\"\">These highlights do not include all the information needed to use LUCIOLAP safely and effectively. See full prescribing information for LUCIOLAP.<\/strong><\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>INDICATIONS AND USAGE<\/strong><strong><\/strong><\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">LUCIOLAP is a poly (ADP-ribose) polymerase (PARP) inhibitor indicated:<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">Ovarian cancer<\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;for the maintenance treatment of adult patients with deleterious or suspected &nbsp;deleterious germline or somatic BRCA-mutated advanced epithelial ovarian, fallopian tube or primary peritoneal cancer who are in complete or partial response to first-line platinum-based chemotherapy. Select patients for therapy based on an FDA-approved companion diagnostic for LUCIOLAP. <\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;in combination with bevacizumab for the maintenance treatment of adult patients with advanced epithelial ovarian, fallopian tube or primary peritoneal cancer who are in complete or partial response to first-line platinum-based chemotherapy &nbsp;and whose cancer is associated with homologous recombination deficiency (HRD)-positive status defined by either:<\/span><\/p>\n<p style=\"text-indent:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;a deleterious or suspected deleterious BRCA mutation, and\/or<\/span><\/p>\n<p style=\"text-indent:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;genomic instability.<\/span><\/p>\n<p style=\"text-indent:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">Select patients for therapy based on an FDA-approved companion diagnostic for LUCIOLAP.<\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;for the maintenance treatment of adult patients with deleterious or suspected deleterious germline or somatic BRCA-mutated recurrent epithelial ovarian, fallopian tube or primary peritoneal cancer, who are in complete or partial response to platinum-based chemotherapy. Select patients for therapy based on an &nbsp;FDA-approved companion diagnostic for LUCIOLAP.<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">Breast cancer<\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;for the adjuvant treatment of adult patients with deleterious or suspected &nbsp;deleterious gBRCAm human epidermal growth factor receptor 2 (HER2)-negative high risk early breast cancer who have been treated with neoadjuvant or adjuvant chemotherapy. Select patients for therapy based on an FDA-approved companion diagnostic for LUCIOLAP.<\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;for the treatment of adult patients with deleterious or suspected deleterious &nbsp;gBRCAm, HER2-negative metastatic breast cancer who have been treated with chemotherapy in the neoadjuvant, adjuvant or metastatic setting. Patients with hormone receptor (HR)-positive breast cancer should have been treated with a prior endocrine therapy or be considered inappropriate for endocrine therapy. Select patients for therapy based on an FDA-approved companion diagnostic for LUCIOLAP. <\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">Pancreatic cancer<\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;for the maintenance treatment of adult patients with deleterious or suspected deleterious gBRCAm metastatic pancreatic adenocarcinoma whose disease has not progressed on at least 16 weeks of a first-line platinum-based chemotherapy regimen. Select patients for therapy based on an FDA-approved companion diagnostic for LUCIOLAP. <\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">Prostate cancer<\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;for the treatment of adult patients with deleterious or suspected deleterious germline or somatic homologous recombination repair (HRR) gene-mutated metastatic castration-resistant prostate cancer (mCRPC) who have progressed following prior treatment with enzalutamide or abiraterone. Select patients for therapy based on an FDA-approved companion diagnostic for LUCIOLAP. <\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;\u2022 &nbsp;in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with deleterious or suspected deleterious BRCA-mutated (BRCAm) metastatic castration-resistant prostate cancer (mCRPC). Select patients for therapy based on an FDA-approved companion diagnostic for LUCIOLAP.<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>DOSAGE AND ADMINISTRATION<\/strong><strong><\/strong><\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022&nbsp;&nbsp;Recommended dosage is 300 mg taken orally twice daily with or without food. See Full&nbsp;Prescribing Information for the recommended duration. <strong><\/strong><\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 &nbsp;Patients receiving LUCIOLAP for mCRPC should also receive a gonadotropin-releasing hormone&nbsp;(GnRH) analog concurrently or should have had bilateral orchiectomy. <\/span><\/p>\n<p style=\"margin-left:28px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 &nbsp;For moderate renal impairment (CLcr 31-50 mL\/min), reduce LUCIOLAP dosage to &nbsp;200 mg&nbsp;orally twice daily.<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>DOSAGE FORMS AND STRENGTHS <\/strong><strong><\/strong><\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">Tablets: 150&nbsp;mg\u00d7120 tablets<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>CONTRAINDICATIONS <\/strong><strong><\/strong><\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">None.<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>WARNINGS AND PRECAUTIONS <\/strong><strong><\/strong><\/span><\/p>\n<p style=\"margin-left:14px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 Myelodysplastic Syndrome\/Acute Myeloid Leukemia (MDS\/AML): Occurred in approximately 1.2% of patients with various BRCAm, gBRCAm, HRR gene-mutated or HRD-positive cancers exposed to LUCIOLAP and the majority of events had a fatal outcome. Monitor patients for hematological toxicity at baseline and monthly thereafter. Discontinue if MDS\/AML is confirmed. <\/span><\/p>\n<p style=\"margin-left:14px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 Pneumonitis: Occurred in 0.8% of patients exposed to LUCIOLAP, and some cases were fatal. Interrupt treatment if pneumonitis is suspected. Discontinue if pneumonitis is confirmed.<\/span><\/p>\n<p style=\"margin-left:14px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 Venous thromboembolism (VTE), including severe or fatal pulmonary embolism (PE), occurred in patients treated with LUCIOLAP. VTE occurred in 8% of patients with mCRPC. Monitor patients for signs and symptoms of VTE and PE and treat as medically appropriate. <\/span><\/p>\n<p style=\"margin-left:14px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 Embryo-Fetal Toxicity: Can cause fetal harm. Advise of the potential risk to a fetus and to use effective contraception. <\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>ADVERSE REACTIONS <\/strong><strong><\/strong><\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">Most common adverse reactions (\u226510%) in clinical trials:<\/span><\/p>\n<p style=\"margin-left:14px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 as a single agent were nausea, fatigue (including asthenia), anemia, vomiting, diarrhea, decreased appetite, headache, dysgeusia, cough, neutropenia, dyspnea, dizziness, dyspepsia, leukopenia, and thrombocytopenia. <\/span><\/p>\n<p style=\"margin-left:14px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 in combination with bevacizumab were nausea, fatigue (including asthenia), anemia, lymphopenia, vomiting, diarrhea, neutropenia, leukopenia, urinary tract infection, and headache. <\/span><\/p>\n<p style=\"margin-left:14px;line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 in combination with abiraterone and prednisone or prednisolone were anemia, fatigue, nausea, diarrhea, decreased appetite, lymphopenia, dizziness, and abdominal pain. <\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>DRUG INTERACTIONS <\/strong><strong><\/strong><\/span><\/p>\n<p style=\"margin-top:2px;margin-right:27px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022&nbsp;&nbsp;Strong or moderate CYP3A inhibitors: Avoid concomitant use. If concomitant use cannot be avoided, reduce LUCIOLAP dosage.<\/span><\/p>\n<p style=\"margin-top:2px;margin-right:27px\"><span style=\"font-size:16px;color:#3f3f3f\">\u2022 &nbsp;Strong or moderate CYP3A inducers: Avoid concomitant use.<\/span><\/p>\n<p style=\"margin-top:2px;margin-right:27px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>USE IN SPECIFIC POPULATIONS <\/strong><strong><\/strong><\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">Lactation: Advise women not to breastfeed.<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\">&nbsp;<\/span><\/p>\n<p style=\"line-height:20px\"><span style=\"font-size:16px;color:#3f3f3f\"><strong>Storage <\/strong><strong><\/strong><\/span><\/p>\n<p><span style=\"font-size:16px;color:#3f3f3f\">Store at 20\u2103&nbsp;to 25\u2103&nbsp;(68\u2109&nbsp;to 77\u2109), excursions permitted between 15\u2103&nbsp;and 30\u2103&nbsp;(59\u2109&nbsp;and 86\u2109) [see USP Controlled Room Temperature]. Protect from moisture.&nbsp;<\/span><\/p>\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>LuciOlap contains olaparib and is supplied as 150 mg tablets in a pack of 120. Please review the full product information with your prescriber. A valid prescription and identity verification are required before ordering.<\/p>","protected":false},"featured_media":1979,"comment_status":"open","ping_status":"closed","template":"","meta":{"advanced_seo_description":"","jetpack_seo_html_title":"","jetpack_seo_noindex":false,"jetpack_seo_schema_type":""},"product_brand":[],"product_cat":[46],"product_tag":[],"class_list":["post-308","product","type-product","status-publish","has-post-thumbnail","product_cat-ovarian-cancer","first","instock","shipping-taxable","purchasable","product-type-simple"],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/product\/308","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/comments?post=308"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/media\/1979"}],"wp:attachment":[{"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/media?parent=308"}],"wp:term":[{"taxonomy":"product_brand","embeddable":true,"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/product_brand?post=308"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/product_cat?post=308"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/luciuspharmacy.com\/ar\/wp-json\/wp\/v2\/product_tag?post=308"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}