Table: q1_q4_2020_prescription_drugs_intro_to_market , manufacturer_name like K*

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z  *

manufacturer_name ndc_number drug_product_description date_introduced_to_market wac_at_introduction marketing_pricing_plan_description marketing_pricing_plan_non_public_indicator estimated_number_of_patients breakthrough_therapy_indicator priority_review_indicator acquisition_date acquisition_price acquisition_price_non_public_indicator acquisition_price_comment general_comments supporting_documents
Karyopharm Therapeutics Inc. 72237010106 XPOVIO (selinexor) 40mg (16 Tablets) 2020-06-22 22000.0000 None 1 9000 None 1 None None None None None None
Karyopharm Therapeutics Inc. 72237010107 XPOVIO (selinexor) 40mg (8 Tablets) 2020-06-22 22000.0000 None 1 9000 None 1 None None None None None None
Karyopharm Therapeutics Inc. 72237010103 XPOVIO (selinexor) 60mg (24 Tablets) 2020-06-22 22000.0000 None 1 9000 None 1 None None None None None None
Kite Pharma, Inc. 71287021901 TECARTUS™ (brexucabtagene autoleucel) 2 × 106CAR-positive viable T cells per kg of body weight, with a maximum of 2 × 108 CAR-positive viable T cells in approximately 68 mL of cell suspension for infusion 2020-07-30 373000.0000 None 1 None 1 1 None None None None The information provided in this report is subject to general limitations and assumptions Kite has shared with OSHPD. The limitations and assumptions address gaps in guidance related to the definition and interpretation of various data elements within New Drug Reports. Additionally, consistent with the relevant statutes and regulations, the information provided in this report is limited to that which Kite believes is in the public domain or otherwise publicly available. Kite is not aware of publicly available information related to the estimated number of patients that may be treated with TECARTUS cell therapy. Consistent with Section 127681(c) of the California Health and Safety Code, Kite is unable to provide an estimated number of patients in its report. Kite has not provided a response to the drug acquisition related data fields for this drug product because Kite developed this drug product. None