![]() |
½ÃÀ庸°í¼
»óÇ°ÄÚµå
1383469
¼¼°èÀÇ ±¸°ºØÇØÁ¤ ½ÃÀå ¿¹Ãø(-2030³â) : Á¦Ç°º°, ¾àÈ¿±ºº°, ÀûÀÀÁõº°, À¯Åëä³Îº° ¹× Áö¿ªº° ºÐ¼®Orally Disintegrating Tablet Market Forecasts to 2030 - Global Analysis By Product, Drug Class, Indication, Distribution Channel and by Geography |
Stratistics MRC¿¡ µû¸£¸é ¼¼°èÀÇ ±¸°ºØÇØÁ¤ ½ÃÀåÀº 2023³â 150¾ï 7,974¸¸ ´Þ·¯·Î 2030³â¿¡´Â 382¾ï 6,971¸¸ ´Þ·¯¿¡ ´ÞÇÒ °ÍÀ¸·Î ¿¹»óµÇ¸ç ¿¹Ãø ±â°£ µ¿¾È 14.23%ÀÇ CAGRÀ» ³ªÅ¸³¾ °ÍÀ¸·Î ¿¹»óµË´Ï´Ù.
±¸°ºØÇØÁ¤, ¼ÓºØÇØÁ¤, ¼Ó¿ëÁ¤, ¼ÓºØÇØÁ¤À̶ó°íµµ ºÒ¸®´Â ±¸°ºØÇØÁ¤Àº ±¸° ³» ¶Ç´Â Çô À§¿¡ ¿Ã·Á³õÀ¸¸é ºü¸£°Ô ¿ëÇØ ¶Ç´Â ºØÇصǴ °íÇü Á¦ÇüÀÔ´Ï´Ù. ¶ÇÇÑ, ±¸° Á¡¸·¿¡¼ ºü¸¥ ¾à¹° Èí¼ö¸¦ °¡´ÉÇÏ°Ô ÇÏ´Â ¼ÓºØÇØÁ¤, ¼ÓºØÇØÁ¤Àº ´Ù¾çÇÑ ±â¼úÀ» È°¿ëÇÑ Á¦Çüȸ¦ ÅëÇØ ½ÇÇöµÇ°í ÀÖÀ¸¸ç, ODTÀÇ Á¦ÇüÈ¿¡´Â À¯È¿¼ººÐÀÇ È¿´ÉÀ» À¯ÁöÇÏ¸é¼ È¯ÀÚ¿¡°Ô ¸¸Á·°¨À» ÁÙ ¼ö ÀÖµµ·Ï ¸À, ¾ÈÁ¤¼º, Á¦Á¶¼ºÀÇ ±ÕÇüÀ» ½ÅÁßÇÏ°Ô °í·ÁÇØ¾ß ÇÕ´Ï´Ù.
FDA(2008)¿¡ µû¸£¸é, ±¸°ºØÇØÁ¤Á¦´Â USPºØÇؽÃÇèÀ» ÅëÇØ 30ÃÊ À̳»¿¡ ºØÇØÇÏ´Â °ÍÀÌ ¹Ù¶÷Á÷ÇÏ´Ù°í ÇÑ´Ù(23). Á¦Á¦ F1°ú F2´Â 30ÃÊ ¹Ì¸¸ÀÇ ºØ±« ½Ã°£À» º¸¿´½À´Ï´Ù.
ÀϺΠ¾à¹°ÀÇ »ý¹°ÇÐÀû ÀÌ¿ë·üÀº ODT¿¡ ÀÇÇØ °³¼±µÉ ¼ö ÀÖ½À´Ï´Ù. Ç÷·ù ³» ¾à¹° ³óµµ°¡ ³ô¾ÆÁö´Â °ÍÀº ±¸° Á¡¸·¿¡¼ ¿ëÇØµÇ¾î °£¿¡¼ ù ¹ø° Åë°ú ´ë»ç¸¦ ÇÇÇÒ ¼ö Àֱ⠶§¹®ÀÔ´Ï´Ù. ¶ÇÇÑ, ODT´Â »ýüÀÌ¿ë·üÀÌ ³·°Å³ª °£ ´ë»ç¸¦ ¸¹ÀÌ ¹Þ´Â ¾à¹°¿¡ ƯÈ÷ À¯¿ëÇϱ⠶§¹®¿¡ ÇöÀç ´Ù¾çÇÑ ÀǾàÇ° Æ÷Æ®Æú¸®¿À¿¡ Æ÷ÇԵǾî ÀÖ½À´Ï´Ù.
¸ðµç ¾à¹°À» ODT·Î ó¹æÇÒ ¼ö ÀÖ´Â °ÍÀº ¾Æ´Õ´Ï´Ù. ÀϺΠ¾à¹°Àº ¸ÀÀÌ ÁÁÁö ¾Ê°Å³ª, ½ÀÇÑ È¯°æ¿¡¼ ¾ÈÁ¤ÀûÀÌÁö ¾Ê°Å³ª, ºü¸£°Ô ¿ëÇصǰųª, °æ±¸ ¾à¹° Àü´Þ ±â¼ú·Î ÇÊ¿äÇÑ ¹°¸®Àû Ư¼ºÀ» °®Áö ¸øÇÒ ¼öµµ ÀÖ½À´Ï´Ù. ¶ÇÇÑ ÀÌ·¯ÇÑ Á¦ÇÑÀ¸·Î ÀÎÇØ Æ¯Á¤ ÈÇÕ¹°À̳ª Ä¡·á±º¿¡ ´ëÇØ ´õ ¸¹Àº ODT¸¦ Á¦°øÇÏ´Â °ÍÀÌ ¾î·Á¿öÁú ¼ö ÀÖ½À´Ï´Ù.
¼Ò¾Æ ÀÇ·á ºÐ¾ß¿¡¼ ODT´Â Å« ÀáÀç·ÂÀ» °¡Áö°í ÀÖ½À´Ï´Ù. ¼Ò¾Æ °Ç°°ü¸®¿¡ ´ëÇÑ ¼ö¿ä°¡ Áõ°¡ÇÔ¿¡ µû¶ó ¾î¸°ÀÌ Ä£ÈÀû Á¦Çü ½ÃÀåµµ È®´ëµÇ°í ÀÖÀ¸¸ç, ODT´Â ¸ÀÀÖ°í ½±°Ô º¹¿ëÇÒ ¼ö ÀÖ´Â ´ë¾ÈÀ» Á¦°øÇÔÀ¸·Î½á ¼Ò¾ÆµéÀÇ º¹¾à ¼øÀÀµµ ¹®Á¦¸¦ ÇØ°áÇÒ ¼ö ÀÖ½À´Ï´Ù. ¶ÇÇÑ, Á¦¾à»çµéÀº ¾Ë·¹¸£±â Ä¡·áÁ¦, Ç×»ýÁ¦ µî ´Ù¾çÇÑ ¼Ò¾Æ¿ë ÀǾàÇ°ÀÇ ODT Á¦ÇüÀ» °³¹ßÇÏ¿© Á¦Ç° ¶óÀξ÷À» È®ÀåÇÒ ¼ö ÀÖ½À´Ï´Ù.
ODT Á¦Á¦´Â ƯÇ㳪 ÁöÀûÀç»ê±ÇÀ¸·Î º¸È£µÇ´Â °æ¿ì°¡ ¸¹¾Æ µ¶Á¡ÀûÀÎ ±â¼úÀ̳ª ¹Ì°¢ ¸¶½ºÅ· Àü·«¿¡ ´ëÇÑ Á¢±ÙÀÌ Á¦ÇÑµÉ ¼ö ÀÖ½À´Ï´Ù. ƯÈ÷ À¯¸íÇÑ ODT Á¦Á¦ÀÇ °æ¿ì, ƯÇã°¡ ¸¸·áµÇ¸é Á¦³×¸¯ ÀǾàÇ° Á¦Á¶¾÷ü°¡ ½ÃÀå¿¡ ÁøÀÔÇÒ ¼ö ÀÖÀ¸¸ç, ÀÌ´Â °¡°Ý Ç϶ô°ú °æÀï ½ÉÈ·Î À̾îÁú ¼ö ÀÖ½À´Ï´Ù. ¶ÇÇÑ ODT ÀǾàÇ° Á¦Á¶¾÷üÀÇ ¼öÀÔµµ À§Çù¹ÞÀ» ¼ö ÀÖ½À´Ï´Ù.
±¸°ºØÇØÁ¤Á¦(ODT) ½ÃÀåÀº Äڷγª19 ÆÒµ¥¹ÍÀ¸·Î ÀÎÇØ ´Ù¾çÇÑ ¿µÇâÀ» ¹Þ°í ÀÖ½À´Ï´Ù. ºñÁ¢ÃË½Ä ÀÚ°¡Åõ¿© Á¦Çü(ODT)ÀÌ À¯ÀÍÇÑ °ÍÀ¸·Î ³ªÅ¸³µÁö¸¸, °ø±Þ¸ÁÀÇ È¥¶õ, ÀÓ»ó½ÃÇèÀÇ Áö¿¬, ±ÔÁ¦ ÀýÂ÷ µîÀ¸·Î ÀÎÇØ ODT Á¦Ç°ÀÇ °³¹ß ¹× º¸±Þ¿¡ Â÷ÁúÀÌ »ý°å½À´Ï´Ù. ¶ÇÇÑ, ÆÒµ¥¹ÍÀº ¿ø°Ý ÀÇ·áÀÇ º¸±ÞÀ» °¡¼ÓÈÇÏ¿© ODT ¾àÇ°ÀÇ ÅÃ¹è ¹× ¿ø°Ý ó¹æÀÇ ¹®À» ¿¾ú½À´Ï´Ù. µµÀü°úÁ¦·Î´Â ÀÇ·á ¿ì¼±¼øÀ§ÀÇ º¯È, ÆÒµ¥¹Í ´ëÀÀÀ» À§ÇÑ ÀÚ¿øÀÇ ÀçºÐ¹è, ÀçÁ¤Àû ¿µÇâ µîÀÌ ÀÖ½À´Ï´Ù. ƯÈ÷ ½Å±Ô ODT ¿¬±¸°³¹ßÀ» À§ÇÑ Àڱݰú ÅõÀÚ¿¡ ¿µÇâÀ» ¹ÌÄ¡°í ÀÖ½À´Ï´Ù.
±¸°ºØÇØÁ¤ ½ÃÀå¿¡¼ °¡Àå ³ôÀº ½ÃÀå Á¡À¯À²À» Â÷ÁöÇÏ´Â ºÎ¹®Àº ¾ç¼ºÀÚ ÆßÇÁ ¾ïÁ¦Á¦ÀÔ´Ï´Ù. ¾ç¼ºÀÚ ÆßÇÁ ¾ïÁ¦Á¦(PPI)·Î ¾Ë·ÁÁø ¾à¹°Àº À§Àå Àå¾Ö, ¼Òȼº ±Ë¾ç, À§½Äµµ ¿ª·ùÁúȯ(GERD) Ä¡·á¿¡ ÀÚÁÖ Ã³¹æµÇ¸ç, PPI´Â À§»ê ºÐºñ¸¦ °¨¼Ò½ÃÄÑ À§»ê ¿ª·ù¿Í °ü·ÃµÈ Áõ»óÀ» ¿ÏÈÇÏ´Â µ¥ µµ¿òÀ» ÁÝ´Ï´Ù. ÀÌ ºÎ¹®ÀÌ ÁÖ¸ñ¹Þ´Â ÀÌÀ¯´Â ¸¸¼º Áúȯ¿¡ ´ëÇÑ PPIÀÇ Àå±âÀûÀÎ »ç¿ë°ú »ê °ü·Ã ÁúȯÀÇ ±¤¹üÀ§ÇÑ È®»ê¿¡ ±âÀÎÇÕ´Ï´Ù. ¶ÇÇÑ, PPI´Â ó¹æ¾à°ú ÀϹÝÀǾàÇ°(OTC)À¸·Îµµ ÆǸŵǰí ÀÖÀ¸¸ç, ½ÃÀåÀÌ È®´ëµÇ°í Àֱ⠶§¹®¿¡ PPI´Â ÇöÀç Á¦¾à¾÷°èÀÇ Áß¿äÇÑ ¿ªÇÒÀ» ÇÏ°í ÀÖ½À´Ï´Ù.
È£Èí±â Áúȯ ºÐ¾ß´Â °¡Àå ³ôÀº CAGR·Î ¼ºÀåÇÒ °ÍÀ¸·Î ¿¹»óµË´Ï´Ù. ´Ù¹ß¼º È£Èí±â °¨¿°, õ½Ä, ¸¸¼ºÆó¼â¼ºÆóÁúȯ(COPD) µî ´Ù¾çÇÑ ÁúȯÀÌ È£Èí±â ÁúȯÀ¸·Î ºÐ·ùµË´Ï´Ù. Èí¿¬, ´ë±â¿À¿°, °í·ÉÈ µîÀÇ ¿äÀÎÀ¸·Î ÀÎÇØ ¼¼°èÀûÀ¸·Î È£Èí±â ÁúȯÀÇ ¹ßº´·üÀÌ ³ô¾ÆÁö¸é¼ »õ·Î¿î Ä¡·á¹ý¿¡ ´ëÇÑ ¼ö¿ä°¡ Áõ°¡ÇÏ°í ÀÖ½À´Ï´Ù. Á¤¹ÐÀÇ·á, »ý¹°ÇÐÀû Á¦Á¦, ÈíÀÔ ±â¼úÀÇ ¹ßÀüÀº È£Èí±â Áúȯ Ä¡·á¿¡ Çõ¸íÀ» ÀÏÀ¸Å°°í ÀÖ½À´Ï´Ù. ¶ÇÇÑ, Äڷγª19ÀÇ ´ëÀ¯ÇàÀ¸·Î È£Èí±â °Ç° ¹®Á¦¿¡ ´ëÇÑ ÀνÄÀÌ ³ô¾ÆÁö¸é¼ ¿¬±¸°³¹ß È°µ¿ÀÌ ´õ¿í È°¹ßÇØÁö°í ÀÖ½À´Ï´Ù.
ºÏ¹Ì°¡ ±¸°ºØÇØÁ¤Á¦ ½ÃÀå¿¡¼ °¡Àå Å« Á¡À¯À²À» Â÷ÁöÇÏ°í ÀÖ½À´Ï´Ù. ºÏ¹ÌÀÇ °·ÂÇÑ ÀÇ·á ½Ã½ºÅÛ, ¸·´ëÇÑ ÀÇ·á ¿¹»ê, ±¤¹üÀ§ÇÑ Á¶»ç °³¹ß, ´Ù¾çÇÑ Áúº´À» ¾Î°í Àִ ȯÀÚÃþÀÌ ÀÌ ºÐ¾ß¿¡¼ ¿ìÀ§¸¦ Á¡ÇÏ°í ÀÖ´Â °ÍÀ¸·Î º¸ÀÔ´Ï´Ù. Á¤±³ÇÑ ÀÇ·á ±â¼ú, °·ÂÇÑ ¿¬±¸ ±â°ü, ÀÇ·á Çõ½ÅÀ» Áß½ÃÇÏ´Â ¹Ì±¹Àº ƯÈ÷ ÀǾàÇ°ÀÇ ¹ßÀü¿¡ Å« ÈûÀ» º¸Å°í ÀÖ½À´Ï´Ù. ¶ÇÇÑ, ºÏ¹Ì´Â »õ·Î¿î ÇコÄɾî À̽´¿¡ ´ëÇÑ Àû±ØÀûÀÎ ´ëÀÀÀ» ÅëÇØ ¼¼°è Á¦¾à »ê¾÷À» ¼±µµÇÏ´Â À§Ä¡¸¦ À¯ÁöÇÏ°í ÀÖ½À´Ï´Ù.
±¸°ºØÇØÁ¤ ½ÃÀåÀº ¾Æ½Ã¾ÆÅÂÆò¾ç¿¡¼ °¡Àå ³ôÀº CAGR·Î ¼ºÀåÇÏ°í ÀÖ½À´Ï´Ù. °æÁ¦ ¹ßÀü, ÀÇ·á ÀÎ½Ä Çâ»ó, ÀÇ·á ¼ºñ½º Á¢±Ù¼º Çâ»ó µî ¿©·¯ ¿äÀÎÀÌ ÀÌ·¯ÇÑ ³î¶ó¿î ¼ºÀå¿¡ ±â¿©ÇÏ°í ÀÖ½À´Ï´Ù. ÇコÄÉ¾î ±â¾÷µéÀÇ ´ë±Ô¸ð ÅõÀÚ·Î ÀÎÇØ ¾Æ½Ã¾ÆÅÂÆò¾çÀº ÀǾàÇ° °³¹ß, ÀÓ»ó½ÃÇè ¹× ÀÇÇÐ ¿¬±¸ÀÇ Áß¿äÇÑ °ÅÁ¡À¸·Î ºÎ»óÇÏ°í ÀÖ½À´Ï´Ù. ¶ÇÇÑ, ÀÌ Áö¿ªÀº »ý¸í°øÇÐ, ½Å¾à, ÇコÄɾî ÀÎÇÁ¶ó¿¡¼ ±Þ¼ÓÇÑ ¹ßÀüÀ» ÀÌ·ç¸ç ¼¼°è Á¦¾à »ê¾÷ÀÇ È®Àå°ú Çõ½ÅÀÇ ÁÖ¿ä Ã˸ÅÁ¦ ¿ªÇÒÀ» ÇÏ°í ÀÖ½À´Ï´Ù.
According to Stratistics MRC, the Global Orally Disintegrating Tablet Market is accounted for $15079.74 million in 2023 and is expected to reach $38269.71 million by 2030 growing at a CAGR of 14.23% during the forecast period. Orally disintegrating tablets, sometimes referred to as melt-in-mouth, fast-dissolving, or fast-disintegrating tablets, are solid dosage forms that, when placed in the oral cavity or on the tongue, dissolve or disintegrate quickly. Moreover, the rapid disintegration and dissolution of these tablets, which enable quick drug absorption through the oral mucosa, are ensured by their formulation, which utilizes a variety of technologies. In order to give patients a satisfying experience while preserving the effectiveness of the active pharmaceutical ingredient, the formulation of ODTs requires a careful balancing act between taste, stability, and manufacturability.
According to the FDA (2008), orodispersible tablets should disintegrate within 30 s using the USP disintegration test [23]. Formulations F1 and F2 showed a disintegration time of less than 30 s.
The bioavailability of some medications may be improved by ODTs. Higher drug concentrations in the bloodstream are the consequence of their dissolution in the oral mucosa, which evades the liver's first-pass metabolism. Additionally, ODTs are now included in a variety of pharmaceutical portfolios because of their particular value for medications with low bioavailability and those that undergo extensive hepatic metabolism.
Every medication cannot be formulated for ODT. Certain medications may not taste well, may not stabilize well in damp environments or dissolve quickly, or may not have the physical qualities needed to be used as oral drug delivery technologies. Furthermore, this restriction might make it more difficult to offer more ODT for particular drug compounds and therapeutic classes.
In pediatric medicine, ODTs offer a great deal of potential. The market for kid-friendly dosage forms has expanded in tandem with the growth in the need for pediatric healthcare. ODTs address the difficulties related to pediatric medication adherence by providing a tasty and simple-to-administer alternative. Moreover, pharmaceutical companies can broaden their product offerings by creating ODT formulations for a variety of pediatric drugs, such as allergy treatments and antibiotics.
Patents and intellectual property rights frequently shield ODT formulations, which can restrict access to exclusive technology and taste-masking strategies. Especially for well-known ODT products, generic manufacturers may enter the market as patents expire, which could lead to price erosion and increased competition. Additionally, the income of ODT drug manufacturers may be threatened by this.
The Orally Disintegrating Tablet (ODT) market has been impacted by the COVID-19 pandemic in a number of ways. Although contactless, self-administered dosage forms (ODTs) have been shown to be beneficial, the development and accessibility of ODT products have been hampered by supply chain disruptions, delays in clinical trials, and regulatory processes. Additionally, the pandemic hastened the adoption of telemedicine, opening doors for home delivery of ODT medications and remote prescribing. Challenges have included shifting healthcare priorities, reallocating resources toward pandemic response efforts, and facing financial ramifications. These have especially affected funding and investment for new ODT research and development.
In the Orally Disintegrating Tablet Market, the segment with the largest market share is proton pump inhibitors. Medications known as proton pump inhibitors (PPIs) are frequently prescribed to treat gastrointestinal disorders, peptic ulcers, and gastroesophageal reflux disease (GERD). They relieve patients experiencing symptoms related to acid reflux by decreasing the production of stomach acid. The prominence of this segment is partly due to the long-term use of PPIs for chronic conditions and the widespread prevalence of disorders related to acidity. Moreover, PPIs are now a significant player in the pharmaceutical industry due to their expanded market reach and availability in both prescription and over-the-counter (OTC) versions.
The respiratory disorders segment is expected to grow at the highest CAGR. A broad spectrum of illnesses is categorized as respiratory disorders, such as multiple respiratory infections, asthma, and chronic obstructive pulmonary disease (COPD). The need for novel treatments is fueled by the rising incidence of respiratory illnesses worldwide, which is a result of factors like smoking, air pollution, and aging populations. Improvements in precision medicine, biologics, and inhalation technologies are revolutionizing the treatment of respiratory illnesses. Furthermore, the COVID-19 pandemic has raised awareness of respiratory health issues and prompted more research and development activities.
In the oral disintegrating tablet market, North America has the largest share. Its strong healthcare system, large healthcare budget, extensive R&D, and sizable patient base with a variety of medical conditions are all considered contributing factors to its dominance in the field. Due to its sophisticated medical technology, strong research institutions, and emphasis on healthcare innovation, the United States in particular is a major force behind pharmaceutical advancements. Moreover, by leading the world's pharmaceutical industry, North America maintains its position thanks to its proactive response to new healthcare challenges.
The oral disintegrating tablet market is growing at the highest CAGR in the Asia-Pacific region. A number of factors, including growing economic development, increased healthcare awareness, and increased access to healthcare services, are responsible for this amazing growth. With major investments from healthcare companies, Asia-Pacific has emerged as a key hub for pharmaceutical development, clinical trials, and medical research. Furthermore, the region is experiencing swift progress in biotechnology, novel pharmaceuticals, and healthcare infrastructure, establishing it as a primary catalyst for expansion and novelty in the worldwide pharmaceutical industry.
Some of the key players in Orally Disintegrating Tablet market include: Takeda Pharmaceutical Company Limited, AstraZeneca, Mylan N.V, Otsuka Pharmaceutical Co., Ltd., Merck & Co., Inc., Pfizer Inc, Johnson & Johnson Services, Inc., Novartis AG, Sun Pharmaceutical Industries Ltd., F. Hoffmann-La Roche Ltd., Eli Lily and Company, GlaxoSmithKline plc., Teva Pharmaceutical Industries Ltd. and Dr. Reddy's Laboratories Ltd., Bausch Health and Bayer AG.
In November 2023, AstraZeneca announced a collaboration and investment agreement with Cellectis to accelerate the development of next-generation therapeutics in areas of high unmet need, including oncology, immunology and rare diseases. Under the terms of the collaboration agreement, AstraZeneca will leverage the Cellectis proprietary gene editing technologies and manufacturing capabilities, to design novel cell and gene therapy products, strengthening AstraZeneca's growing offering in this space.
In May 2023, Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, announced today that it has entered into a worldwide collaboration and license agreement with Cellular Biomedicine Group Inc. (CBMG) to develop, manufacture and commercialize next-generation chimeric antigen receptor (CAR) T-cell therapies for the treatment of B-cell malignancies.
In January 2023, Takeda announced that it has entered into an exclusive licensing agreement with HUTCHMED (China) Limited and its subsidiary HUTCHMED Limited, for the further development and commercialization of fruquintinib outside of mainland China, Hong Kong and Macau.