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Special Report                                                                                                                                                                 Special Report



                                                                                                                        genetic  disorder that prevents the   (crinecerfont)  for treating classic  candidates  are projected  to make up
                                                                                                                        body from breaking down fats;     congenital  adrenal  hyperplasia, a  20%  of  global  pipeline  forecast  sales
                                                                                                                       Ispen’s  Iqirvo  (elafi branor)  for   group  of  hereditary genetic dis-  over the rest of this decade  – in line
                                                                                                                        treating primary biliary cholangitis   orders affecting the adrenal glands;  with the category’s share of 2030 pre-
                                                                                                                        (a rare liver disease) in combination    Servier’s Voranigo  (vorasidenib)  scription pharmaceutical sales, accord-
                                                                                                                        with ursodeoxycholic acid;        for  treating  Grade  2  astrocytoma  ing to the Evaluate report.
                                                                                                                       ITF Therapeutics’  (Italfarmaco)   or oligodendroglioma, two types of
                                                                                                                        Duvyzat (givinostat)  for treating   low-grade brain tumors;        However, as the  Evaluate  report
                                                                                                                        Duchenne muscular dystrophy,  a    Syndax Pharmaceuticals’ Revuforj  points out, there are certain policy un-
                                                                                                                        severe, inherited disease that causes   (revumenib) for treating relapsed or  certainties  in the US  that may affect
                                                                                                                        progressive muscle weakness and   refractory acute leukemia;     forecasts for bio/pharmaceuticals over-
                                                                                                                        degeneration;                    Vertex  Pharmaceuticals’  Alyftrek  all and orphan drugs specifi cally. These
                                                                                                                       Jazz   Pharmaceuticals’   Ziihera   (vanzacaftor, tezacaftor, and deuti-  relate to staffi ng and funding levels at
                                                                                                                        (zanidatamab-hrii)  for  treating  vacaftor) for treating cystic fi brosis;  the US Food and Drug Administration
                                                                                                                        previously  treated, unresectable or    X4 Pharmaceuticals’ Xolremdi  to facilitate  product development  and
                                                                                                                        metastatic HER2-positive (IHC 3+)   (mavorixafor)  for  treating  WHIM  reviews, US government  funding
        Source: Centre for Drug Evaluation and Research, US Food and Drug Administration                                biliary tract cancer, a rare and ag-  syndrome (warts, hypogammaglobu-  under the National Institutes of Health
                                                                                                                        gressive type of cancer that affects   linemia  (low  levels of immuno-  and other programs that support early
                              Fig. 3: Large Bio/Pharma companies: New Ophan Drug Approvals in 2024*                     the organs of the biliary  system,   globulins), infections, and myelo-  drug research and development,  and
       companies, and 18, or 69%, were from   the body’s  immune system attacks   for  treating esophageal squamous     which includes the gallbladder and   kathexi  (a reduction of circulating  potential changes to drug pricing mea-
       mid-to-smaller companies.           the small bile ducts in the liver;   cell carcinoma;                         bile ducts;                       white blood cells);and         sures under the Infl ation Reduction Act
                                           Merck & Co.’s Winrevair (sotater-    BridgeBio  Pharma’s Attruby  (aco-    Merus’ Bizengri (zenocutuzumab-    Zerva  Therapeutics’  Miplyffa  (ari-  (IRA), which included the creation of
          Eight  large bio/pharma  compa-  cept-csrk) for treating pulmonary   ramidis) for  treating cardiomyo-        zbco) for treating certain forms of   moclomol), for  treating Niemann-  the Medicare Prescription Drug Nego-
       nies – Amgen, Astellas, AstraZeneca,   arterial hypertension;         pathy of wild-type or variant trans-       unresectable or  metastatic non-  Pick disease type C, a rare neurode-  tiation Program,  which  authorized the
       Gilead Sciences, Merck & Co., Novo    Novo  Nordisk’s  Alhemo  (conci-  thyretin-mediated amyloidosis,  a       small cell lung cancer and pancreatic   generative disorder.     US government to negotiate prices for
       Nordisk, Pfi zer, and Roche – each had   zumab-mtci) for  preventing or  re-  progressive heart condition where   cancer in patients with a rare gene-                             certain prescription drugs under Medi-
       one new orphan drug approval in 2024   ducing the frequency of bleeding   misfolded transthyretin proteins       tic alteration, NRG1 fusion;   A look ahead                      care, the US federal  health  insurance
       (see Figure 3).                     episodes in patients with hemophilia   accumulate as  amyloid deposits  in     Neurocrine Biosciences’ Crenessity   On a pipeline  basis, orphan drug  program for people 65 or older.
                                           A or B;                           the heart muscle;
          New drug approvals from the large    Pfi zer’s  Hympavzi  (marstacimab-   Day One Biopharmaceuticals’
       bio/pharmaceutical companies in 2024   hncq) also for preventing or reduc-  Ojemda (tovorafenib) for treating           Chemical Weekly | Import-Export Data
       were:                               ing bleeding episodes related to   relapsed or refractory pediatric low-
         Amgen’s Imdelltra (tarlatamabdlle)   hemophilia A or B;            grade glioma (i.e., a brain tumor);
          for  treating  extensive  stage    Roche’s Piasky (crovalimab-akkz)    Geron’s  Rytelo  (imetelstat)  for                    Market Surveys | Directories
          small-cell lung cancer;          for treating paroxysmal nocturnal   treating  low to intermediate-1
         Astellas’s  Vyloy  (zolbetuximab-  hemoglobinuria,  a rare blood dis-  risk myelodysplastic  syndromes, a                    Business Forums | Expositions
          clzb)  in  combination  with  fl uoro-  ease that causes red blood cells to   group of progressive bone marrow
          pyrimidine and platinum-containing   break down.                   disorders;
          chemotherapy  as  a  fi rst-line  treat-                           Incyte’s Niktimvo (axatilimab-csfr)      The only organisation in India catering exclusively to the needs of the entire chemical industry
          ment of adults with locally  ad-  Eighteen mid-to-small bio/pharma-  for treating chronic graft-versus-
          vanced unresectable or metastatic  ceutical companies had a new    host disease after failure of at least                                                Contact:
          HER2-negative  gastric  or  gastro-  orphan  drug  approval  in  2024.  The   two prior lines of systemic therapy;
          esophageal  junction  adenocar-  companies and products are outlined    IntraBio’s  Aqneursa  (levacetylleu-                   SEVAK PUBLICATIONS PVT. LTD.
          cinoma;                        below:                              cine) for treating Niemann-Pick dis-
         AstraZeneca’s  Voydeya  (danicopan)    Ascendis Pharma’s Yorvipath (palo-  ease type C, a rare genetic disease                 602-B, Godrej Coliseum, K.J. Somaiya Hospital Road,
          for treating extravascular hemolysis   pegteriparatide)  for treating hypo-  resulting  in progressive neurologi-                           Behind Everard Nagar, Sion (E),
          with paroxysmal nocturnal hemo-  parathyroidism,  a rare disease   cal  symptoms and organ dysfunc-                                                 Mumbai 400 022.
          globinuria, a rare blood disease;  where the parathyroid glands    tion;
         Gilead  Sciences’  Livdelzi  (sela-  behind the thyroid do not produce    Ionis  Pharmaceuticals’Tryngolza                                  Phone: +91-22-24044471 / 72
          delpar) for treating primary biliary   enough parathyroid hormone;  (olezarsen) for  treating familial                                  Email: admin@chemicalweekly.com
          cholangitis,  a liver disease where    BeOne’s  Tevimbra  (tislelizumabjsgr)   chylomicronemia syndrome, a rare


       164                                                                      Chemical Weekly  May 27, 2025        Chemical Weekly  May 27, 2025                                                                   165


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