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Actual Study Start Date : March 16, 2022

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Jefferies Global Healthcare Conference Presentation Information

Format: Live presentation with webcast link

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Date: Thursday, June 8, 2023

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clinicaltrials.gov/ct2/show/NCT03349060?term=NCT03349060&draw=2&rank=1

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The trio all have late-stage therapies with blockbuster potential.

89bio (ETNB 4.17%), Karuna Therapeutics (KRTX 3.38%), and Morphic Therapeutics (MORF 1.57%) are clinical-stage biotech companies that make attractive buyout targets. Their financial positions may not be great, as they all have little revenue, but they have promising potential blockbuster therapies in their pipelines.

Financing has become more difficult lately for small and mid-sized biotechs. Facing big expenses to fund research and marketing of their drugs, these companies often turn to licensing deals, partnerships, and outright buyouts to see their blockbusters to the finish line.

They are all trading below what they would be if they were profitable companies, but that provides an opportunity for larger pharmaceutical companies and for investors. It allows a chance for a larger company to buy a de-risked asset and investors who think long-term can get in now on a stock that will likely jump if it gets a buyout offer.

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89bio (ETNB 4.17%)¡BKaruna Therapeutics (KRTX 3.38%) ©M Morphic Therapeutics (MORF 1.57%) ¬OÁ{§É¶¥¬qªº¥Íª«§Þ³N¤½¥q¡A¬O¦³§l¤Þ¤Oªº¦¬ÁʥؼСC ¥L­Ìªº°]°Èª¬ªp¥i¯à¨Ã¤£¦n¡A¦]¬°¥L­Ìªº¦¬¤J³£«Ü¤Ö¡A¦ý¥L­ÌªººÞ¹D¤¤¦³«Ü¦³§Æ±æªº¼ç¦b­«½S¬µ¼uÀøªk¡C

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89bio¡¦s top therapy is getting close to approval

89bio presents strong potential as a buyout candidate. The company¡¦s stock is up more than 28% so far this year, thanks to positive news regarding its lead pipeline candidate.

The clinical-stage biotech company specializes in therapies to treat cardio-metabolic and liver diseases. 89bio¡¦s potential blockbuster drug is pegozafermin, which did well in a phase 2b trial to treat nonalcoholic steatohepatitis (NASH) patients. The disease is a form of nonalcoholic fatty liver disease that causes inflammation of the liver and liver damage and can lead to fibrosis, or scarring of the liver. It can also lead to cirrhosis, permanent scarring of the liver that can lead to liver cancer. Nearly 35.5% of those who are overweight have NASH, according to a recent meta-analysis published by the National Library of Medicine.

Pegozafermin¡¦s next step is two phase 3 trials to treat NASH, which has a relatively large target market. There are no Food and Drug (FDA)-approved therapies yet to treat the disease, which affects 5% of adults in the U.S., according to the American Liver Foundation.

Pegozafermin is also being looked at to treat severe hypertriglyceridemia (SHTG), when a person has high levels of triglycerides, which could lead to atherosclerosis, heart disease and acute pancreatitis. In a phase 2 study, pegozafermin significantly reduced triglycerides. SHTG affects up to 4 million people in the U.S.

89bio has no revenue and lost $102 million last year. It recently raised cash by selling $275 worth of stock, as it had only $188.2 million at the end of 2022.

89bioªº³»¯ÅÀøªk§Y±NÀò§å

89bio §@¬°¦¬ÁÊ­Ô¿ï¤H¨ã¦³±j¤jªº¼ç¤O¡C ¥Ñ©ó¦³Ãö¨ä¥D­n­Ô¿ïÃĪ«ªº§Q¦n®ø®§¡A¸Ó¤½¥qªÑ»ù¤µ¦~¨´¤µ¤w¤Wº¦¶W¹L 28%¡C

³o®aÁ{§É¶¥¬qªº¥Íª«§Þ³N¤½¥q±Mªù±q¨ÆªvÀø¤ßŦ¥NÁ©M¨xŦ¯e¯fªºÀøªk¡C 89bio ªº¼ç¦b­«½SÃĪ«¬O pegozafermin¡A¥¦¦bªvÀø«D°sºë©Ê¯×ªÕ©Ê¨xª¢ (NASH) ±wªÌªº 2b ´Á¸ÕÅ礤ªí²{¨}¦n¡C ³oºØ¯e¯f¬O«D°sºë©Ê¯×ªÕ¨xªº¤@ºØ§Î¦¡¡A·|¤Þ°_¨xŦª¢¯g©M¨x·l¶Ë¡A¨Ã¥i¯à¾É­PÅÖºû¤Æ©Î¨xŦ½I²ª§Î¦¨¡C ¥¦ÁÙ¥i¯à¾É­P¨xµw¤Æ¡A§Y¨xŦ¥Ã¤[©Ê¬Í²ª¡A±q¦Ó¾É­P¨xÀù¡C ®Ú¾Ú°ê®aÂå¾Ç¹Ï®ÑÀ]³Ìªñµoªíªº¤@¶µîPµÑ¤ÀªR¡Aªñ 35.5% ªº¶W­«ªÌ±w¦³ NASH¡C

Pegozafermin ªº¤U¤@¨B¬OªvÀø NASH ªº¨â¶µ 3 ´Á¸ÕÅç¡A¨ä¥Ø¼Ð¥«³õ¬Û¹ï¸û¤j¡C ®Ú¾Ú¬ü°ê¨xŦ°òª÷·|ªº¼Æ¾Ú¡A¥Ø«eÁÙ¨S¦³­¹«~©MÃĪ« (FDA) §å­ãªºÀøªk¨ÓªvÀø³oºØ¼vÅT¬ü°ê 5% ¦¨¦~¤Hªº¯e¯f¡C

Pegozafermin ¤]³Q¥Î©óªvÀøÄY­«ªº°ª¥Ìªo¤Tà­¦å¯g (SHTG)¡A·í¤@­Ó¤Hªº¥Ìªo¤Tà­¤ô¥­«Ü°ª®É¡A³o¥i¯à¾É­P°Ê¯ßµ°¼Ëµw¤Æ¡B¤ßż¯f©M«æ©Ê¯Ø¸¢ª¢¡C ¦b¤@¶µ 2 ´Á¬ã¨s¤¤¡Apegozafermin ÅãµÛ­°§C¤F¥Ìªo¤Tà­¡C SHTG ¼vÅT¤F¬ü°ê¦h¹F 400 ¸U¤H¡C

89bio ¨S¦³¦¬¤J¡A¥h¦~Á«·l 1.02 »õ¬ü¤¸¡C ¥¦³Ìªñ³q¹L¥X°â»ù­È 2.75 »õ¬ü¤¸(3/23)ªºªÑ²¼Äw¶°²{ª÷¡A¦]¬°¨ì 2022 ¦~©³¥¦¥u¦³ 1.882 »õ¬ü¤¸¡C

Karuna is in a race to develop a schizophrenia drug

Karuna Therapeutics focuses on therapies to treat psychiatric and neurological conditions. The clinical-stage biotech is on track for its first marketed therapy and its shares are up more than 62% over the past year, but flat so far this year.

The company said it plans to file a New Drug Application (NDA) with the FDA midway through this year for KarXT, a muscarinic agonist, to treat schizophrenia. The drug is a combination of xanomeline and trospium chloride. The advantage for KarXT is it seems to have fewer side effects than many antipsychotic drugs. The target group for KarXT could be quite large. According to the World Health Organization, 24 million people worldwide, roughly 1 in 300, have the disease. and drugs used for schizophrenia often can migrate into other applications, such as dementia-related psychosis.

In preparation for a potential launch of KarXT, Karuna recently sold $400 million worth of stock. At the end of 2022, it said it had $1.1 billion in cash, enough to fund operations into 2025. Last year, the company had $10.6 million in collaboration revenue but it lost $274.9 million.

One concern for Karuna is that another schizophrenia drug is on the horizon, emraclidine, from Cerevel Therapeutics, which is in phase 2 trials. However, it is at least two years away from approval. It might make sense for a larger company to buy Karuna now before its Kar-XT is approved.

One potential suitor could be Eli Lilly, which sold the rights to xanomeline to Karuna in the first place. Biogen and Jazz Pharmaceuticals, both of which are active in neurological therapies, might also make sense as suitors.

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Karuna ªº¤@­Ó¾á¼~¬O¡A¥t¤@ºØºë¯«¤Àµõ¯gÃĪ«§Y±N¤W¥«¡A¨Ó¦Û Cerevel Therapeutics ªº emraclidine ¥¿³B©ó 2 ´Á¸ÕÅ綥¬q¡C ¦ý¬O¡A¶ZÂ÷§å­ã¦Ü¤ÖÁÙ¦³¨â¦~®É¶¡¡C ¦b Karuna ªº Kar-XT Àò±o§å­ã¤§«e¡A¤@®a¤j¤½¥q²{¦bÁʶR Karuna ¥i¯à¬O¦³·N¸qªº¡C

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Immunology drug makes Morphic a hot commodity

Morphic focuses on oral integrin drugs to treat chronic diseases, including fibrosis, cancer, and autoimmune, cardiovascular, and metabolic diseases. The company¡¦s stock is up more than 77% this year, thanks to positive news regarding its lead ulcerative colitis (UC) therapy, MORF-57.

In a phase 2a trial with UC patients, the drug was responsible for complete remissions in 26% of patients. The twice-daily oral pill has the potential to match the efficacy of Entyvio, regarded as a $5 billion a year UC and Crohn¡¦s Disease therapy from Takeda Pharmaceutical. Through nine months this year, Entyvio has posted sales of 547.9 billion yen ($4.1 billion).

Morphic said it has $421 million in cash as of March 31, enough to fund operations into 2026, giving it plenty of time to develop MORF-057.

In the first quarter of 2023, the company had a net loss of $36.1 million, with collaboration revenue of $500,000.

Companies such as Morphic that specialize in immunology disorders have become frequent buyout targets. Merck just spent $10.8 billion for Prometheus Biosciences and in 2022, Pfizer completed a $6.7 billion deal to buy Arena Pharmaceuticals

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HC Wainwright & Co. Maintains Buy on ASLAN Pharma, Lowers Price Target to $17

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Connect Biopharma Reports Full Year 2022 Financial Results and Provides Business Update

Connect Biopharma Holdings Limited

Wed, April 12, 2023 at 4:05 AM GMT+8

Anticipated Upcoming Milestones

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China pivotal trial: The Company believes it is on track to complete the 36-week stage 2 maintenance phase of the trial in patients with severe-to-moderate AD in the second half of 2023. This stage of the trial includes a once-a-month (Q4W) dosing regimen. Based on feedback received from the CDE, the Company plans to submit an NDA by the end of the first quarter of 2024 for potential approval in 2025.

Global Phase 3 program: The Company is seeking strategic partnerships to advance this product candidate to the next phase of clinical development with potential global and regional partners to provide the necessary infrastructure and deliver a differentiated therapeutic program with improved efficacy and dosing convenience.

finance.yahoo.com/news/connect-biopharma-reports-full-2022-200500465.html

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1.Lebrikizumab 250mg Q2W x16¶gx2b

44.6//44.0//60.6//81.0//72.1

2.CBP201 300mg Q2wx16¶gx2b

28.1//24.6//47.4//54.4//63.0

3.ASLAN004 600mg QWx8¶gx1b mITT

44//38//69//81//65¤@¤@mITT

4.ASLAN004 600mgxQWx8 ¶g1bxITT

32//27//50//77//61¤@¤@ITT

2021/09/27 1b¸Ñª¼³ø§i

ir.aslanpharma.com/static-files/da4bc98e-9b9d-4add-8d6b-b66b427f76e8

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¬Ý¹êÅç²Õªº¤GªÌ®t¶Z¡A§ó¯à¤À¿ëÀø®ÄÅãµÛ®t²§¡A¤×¨ä¬ÝIGA0,1/EASI90 ¤GÃĤñªñ50%¡C

Lebrikizumab ¼Æ¾Ú¤w±µªñDupilumab ¤T´Á¼Æ¾Ú¡A¤ÏÆ[CBP201 ¬Û®t¬Æ»·¡C

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Lebrikizumab vs CBP-201 AD 2b

1.Lebrikizumab AD 2b

clinicaltrials.gov/ct2/show/results/NCT03443024

IGA0,1//EASI90//EASI75//EASI50//EASI¥­§¡­°´T

³æ¦ì:%

250 mg Q2W N=75 44.6**//44.0***//60.6***//81.0***//72.1***

250 mg Q4W N=73 33.7*//36.1**//56.1**//77.0**//69.2**

125 mg Q4W N=80 26.6//26.1//43.3//66.4//62.3*

¹êÅç²Õ¥­§¡. 34.8//35.2//53.1//74.6//67.7

¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X¡X-

Placebo N=52 15.3//11.4//24.3//45.8//41.1

--------------------------------------------------------

Á`¥­§¡ 31.2//30.8//47.7//69.2//62.8

*P<0.05, **P<0.01, ***P<0.001 vs placebo

¡X¡X¡X¡X¡X­×¥¿¹ï·Ó²Õ¤Î¥­§¡ªºIGA0,1¡X¡X¡X¡X+

2.CBP-201 AD 2b

www.globenewswire.com/news-release/2022/01/05/2361507/0/en/Connect-Biopharma-Reports-Detailed-Positive-Dataset-from-the-Global-Phase-2b-Trial-of-CBP-201-in-Adult-Patients-with-Moderate-to-Severe-Atopic-Dermatitis.html#:~:text=CBP%2D201%20was%20well%20tolerated,biologic%20standard%20of%20care%20therapy.

IGA0,1//EASI90//EASI75//EASI50//EASI¥­§¡­°´T

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300 mg Q2W N=57 28.1*//24.6//47.4***//54.4*//63.0***

300 mg Q4W N=56 21.4//25.0*//41.1**//62.5**//65.4***

150 mg Q2W N=57 15.8//14.0//40.4**//52.2*//57.5**

¹êÅç²Õ¥­§¡¡C 21.8//21.2//46.9//56.3//61.9

¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@¤@

Placebo N=56 10.7//10.7//14.3//33.9//40.7⋯⋯¤@¤@¤@

--------------------------------------------------------

Á`¥­§¡ 19.0/21.1//35.8//50.8//56.7.¡X¡X¡X¡X¡X¡X¡X-(­×¥¿IGA0¡A1¬°19.0)

*P<0.05, **P<0.01, ***P<0.001 vs placebo

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©Î³\·|¤Ö¤Ö¶q¥[½X§a¡A´Á«Ý·à¤l¤C¤ë°fÂà³Ó

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­×¥¿¤@l

¥Ñ¥H¤UªºÁ{§É¸ê°T,¤GªÌ¦U«ü¼ÐÀø®Ä¥­§¡¼Æ¦nÃa®t«Ü¦h!

ASLN ¤½¥q¥²°Ñ¦ÒLebrikizumab 2b ¸ê®Æ¥h¦V¥|¤j¨p¶ÒªÌ»¡©ú¤Î¼ÒÀÀASLAN004 2b 80%¬ù240¤H/5²Õ.

¨ä¤¤¹ï·Ó²Õ¥i§¹¥þ°Ñ·Ó.

¼ÒÀÀ¤§¼Æ¾Ú¥² >=Lebrikizumab 2b ¤~·|¥I¨p¶Ò2000¸U¬ü¤¸(6»õ¥x¹ô)

­Y¼Æ¾Ú±µªñCBP201 2b,«h¥²¥X²M­ì¦³«ùªÑ,

(­ì³Ì¤jªÑªF­ð¸ê¥»­ì«ùªÑ5360¤dªÑADR 1:5,

¥»¦¸¥t¼W¥[7760¤dªÑADR 1:5»{ªÑ)

---------------------------------------------------

Lebrikizumab vs CBP-201 AD 2b

1.Lebrikizumab AD 2b

clinicaltrials.gov/ct2/show/results/NCT03443024

IGA0,1//EASI90//EASI75//EASI50//EASI¥­§¡­°´T

³æ¦ì:%

250 mg Q2W N=75 44.6**//44.0***//60.6***//81.0***//72.1***

250 mg Q4W N=73 33.7*//36.1**//56.1**//77.0**//69.2**

125 mg Q4W N=80 26.6//26.1//43.3//66.4//62.3*

Placebo N=52 15.3//11.4//24.3//45.8//41.1

--------------------------------------------------------

¥­§¡ 31.2//30.8//47.7//69.2//62.8

*P<0.05, **P<0.01, ***P<0.001 vs placebo

¡X¡X¡X¡X¡X­×¥¿¹ï·Ó²Õ¤Î¥­§¡ªºIGA0,1¡X¡X¡X¡X+

2.CBP-201 AD 2b

www.globenewswire.com/news-release/2022/01/05/2361507/0/en/Connect-Biopharma-Reports-Detailed-Positive-Dataset-from-the-Global-Phase-2b-Trial-of-CBP-201-in-Adult-Patients-with-Moderate-to-Severe-Atopic-Dermatitis.html#:~:text=CBP%2D201%20was%20well%20tolerated,biologic%20standard%20of%20care%20therapy.

IGA0,1//EASI90//EASI75//EASI50//EASI¥­§¡­°´T

³æ¦ì:%

300 mg Q2W N=57 28.1*//24.6//47.4***//54.4*//63.0***

300 mg Q4W N=56 21.4//25.0*//41.1**//62.5**//65.4***

150 mg Q2W N=57 15.8//14.0//40.4**//52.2*//57.5**

Placebo N=56 10.7//10.7//14.3//33.9//40.7⋯⋯¤@¤@¤@¤@¤@¤@¤@¡]­×¥¿IGA0,1 ¬°10.7)

--------------------------------------------------------

¥­§¡ 19.0/21.1//35.8//50.8//56.7.¡X¡X¡X¡X¡X¡X¡X-(­×¥¿IGA0¡A1¬°19.0)

*P<0.05, **P<0.01, ***P<0.001 vs placebo

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¥Ñ¥H¤UªºÁ{§É¸ê°T,¤GªÌ¦U«ü¼ÐÀø®Ä¥­§¡¼Æ¦nÃa®t«Ü¦h!

ASLN ¤½¥q¥²°Ñ¦ÒLebrikizumab 2b ¸ê®Æ¥h¦V¥|¤j¨p¶ÒªÌ»¡©ú¤Î¼ÒÀÀASLAN004 2b 80%¬ù240¤H/5²Õ.

¨ä¤¤¹ï·Ó²Õ¥i§¹¥þ°Ñ·Ó.

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­Y¼Æ¾Ú±µªñCBP201 2b,«h¥²¥X²M­ì¦³«ùªÑ,

(­ì³Ì¤jªÑªF­ð¸ê¥»­ì«ùªÑ5360¤dªÑADR 1:5,

¥»¦¸¥t¼W¥[7760¤dªÑADR 1:5»{ªÑ)

---------------------------------------------------

Lebrikizumab vs CBP-201 AD 2b

1.Lebrikizumab AD 2b

clinicaltrials.gov/ct2/show/results/NCT03443024

IGA0,1//EASI90//EASI75//EASI50//EASI¥­§¡­°´T

³æ¦ì:%

250 mg Q2W N=75 44.6**//44.0***//60.6***//81.0***//72.1***

250 mg Q4W N=73 33.7*//36.1**//56.1**//77.0**//69.2**

125 mg Q4W N=80 26.6//26.1//43.3//66.4//62.3*

Placebo N=52 15.3//11.4//24.3//45.8//41.1

--------------------------------------------------------

¥­§¡ 31.2//30.8//47.7//69.2//62.8

*P<0.05, **P<0.01, ***P<0.001 vs placebo

2.CBP-201 AD 2b

www.globenewswire.com/news-release/2022/01/05/2361507/0/en/Connect-Biopharma-Reports-Detailed-Positive-Dataset-from-the-Global-Phase-2b-Trial-of-CBP-201-in-Adult-Patients-with-Moderate-to-Severe-Atopic-Dermatitis.html#:~:text=CBP%2D201%20was%20well%20tolerated,biologic%20standard%20of%20care%20therapy.

IGA0,1//EASI90//EASI75//EASI50//EASI¥­§¡­°´T

³æ¦ì:%

300 mg Q2W N=57 28.1*//24.6//47.4***//54.4*//63.0***

300 mg Q4W N=56 21.4//25.0*//41.1**//62.5**//65.4***

150 mg Q2W N=57 15.8//14.0//40.4**//52.2*//57.5**

Placebo N=56 15.3//10.7//14.3//33.9//40.7

--------------------------------------------------------

¥­§¡ 20.2//21.1//35.8//50.8//56.7

*P<0.05, **P<0.01, ***P<0.001 vs placebo

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1.´î¸ê2¦¸«ùªÑ§C¥[½X©é¤F

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004 2b AD

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(¥H¤W¬°­É¥ÎLebrikizumab 2b/¤T´Á¼Æ¾Ú)

2b°ªÀÉÀø®Ä¹LÃö¡B¤T´ÁÀø®Ä©M¹ï·Ó组®t²§·|©Ô§ó¤j¡B

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MOS©ÎORR¬°¥D­n«ü¼Ð¡B

统计¤W¹êÅç组Àø®Ä/¹ï·Ó组Àø®Ä>150%¡Bp­È´N·|<0.05¹LÃö¡D

ADªº°ªÀø®ÄDupilumab/Lebrikizumab©M¹ï·Ó组ªºÀø®Ä¤ñ¬ù3~4­¿¤§¶¡¡B

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µ²½×¡GAD Á{§É2b¡BIGA0,1Àø®Ä©M¹ï·Ó组¤ñ­È3­¿¡B¤T´ÁÁ{§É/ÃÄ证´N§ä¤£¨ì²z¥Ñ¤£¹LÃö¡D

004ªº»ù­È¡B­n¬Ý¬O¤£Àø®ÄIGA0,1>52%/15%

¤~¯à¦³¾÷·|°ª©ó¨é°Ó¥Ø¼Ð»ù

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HIV ¤G°w¾¯¡Aªø®Ä¤G­Ó¤ë¥´¤@¦¸°w¡A¸ê°T¾ã²z

1. CABENUVA 600mg/900mg ¨C¤G¤ë¤@°w¡AÁv¦Ù¦×ª`®g¡A¥ýªA¨â­Ó¤ëªº¤GºØ¤fªAÃĪ«

¦~¶O¥Î¡×1114x3x6¦¸¡×20¡A052¬ü¤¸¡C¤Q ¨â­Ó¤ëªº¤fªAÃÄCabotegravir 30 mg once daily782*2=1562¤QRilpivirine 25 mg once daily 1431*2=2862

¦X­p¡×24¡A476¬ü¤¸¡þ¦~¤@¤@¤@¶O¥Î«D±`«K©y¡C

Recommended Every-2-Month Dosing Schedule: Initiate injections of CABENUVA (600 mg of cabotegravir and 900 mg of rilpivirine) on the last day of current antiretroviral therapy or oral lead-in for 2 consecutive months and continue with injections of CABENUVA every 2 months thereafter. (2.5)

For gluteal intramuscular injection only ¶È¨ÑÁv¦Ùª`®g

www.accessdata.fda.gov/drugsatfda_docs/label/2022/212888s005s006lbl.pdf

www.drugs.com/price-guide/cabenuva

200mg/300mg/ml

¨C³æ¦ì1114¬ü¤¸

Cabenuva intramuscular suspension, extended release

2021¦~¤W¥«¡A¦ô2026¦~¡A¦~¾P26»õ¬ü¤¸

2¡ATMB-365 and TMB-380 in Suppressed HIV-1 Infected Individuals

clinicaltrials.gov/ct2/show/NCT05275998?term=Tmb365+tmb380&draw=2&rank=1

2600mg or 3600mg or 4800mg¨C¤G¤ë¡AÀR¯ßª`®g¤@¦¸¡A

1.2600mgx6=15¡A600mg/¦~¡A15600/400x3024=117¡A936¬ü¤¸¡C

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3¡A4800mgx6=28¡A800mg/¦~¡A28¡A800/400*3024=217¡A728¬ü¤¸/¦~

Trogarzo Prices, Coupons and Patient Assistance Programs

Trogarzo (ibalizumab) is a member of the miscellaneous antivirals drug class and is commonly used for HIV Infection.

The cost for Trogarzo intravenous solution (uiyk 200 mg/1.33 mL) is around $3,024 for a supply of 2.66 milliliters, depending on the pharmacy you visit

www.drugs.com/price-guide/trogarzo

°²³]TMB360/380»ù®æ=TMB355

200mg/1.33x2¡×3024¬ü¤¸

3¡A¥Ñ¤Wµû¦ô¡ATMB360/380 ³J¥Õ½èÃÄ¡A¶W¯Å¶Q¡A­n·m«e缐ªºHIV ÃĪ«¡H¡HÄv¿ï©w¦ì¡H¥BÂùÃIJz½×¤WÃĶO¶Q©óTMB355

¦Ó¾¯¶q°ª»ÝÀR¯ßª`®g¡A

µLªk¦pCABENUVA 600mg/900mg ¨C¤G¤ë¤@°w¡AÁv¦Ù¦×ª`®g¡A¨ú¦^®a¦Û§Úª`®g¡C

¤T´Á¤G­ÓÁ{§É¡A¦U°µ500¤H¡A¦X­p1000¤H¡A48¶g¡C

¨C¤H¶O¥Î¦ô15¡ã20¸U¬ü¤¸x1000¤H¡×1¡A5¡ã2 »õ¬ü¤¸Á{§É¶O¥Î¶]¤£±¼¡C

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¦¨¥\ªºªº·sÃĤ½¥q³Ð¿ì¤H¡A´¿¬ãµoª¢¯g©M¯«¸g¨t²Î¾AÀ³¯g·sÃıÂÅv12.5»õ¬ü¤¸ªºMr.Schonharting,

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3/24 ¨p¶Ò(§t»{ªÑÅv)ªº¦ÛµM¤H Mr. Schönharting,

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---------------------------

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The business address of Mr. Schönharting

is c/o NB Capital, Oestergade 24A, 1100 Copenhagen K, Denmark.

ir.aslanpharma.com/static-files/8ef0bdc0-36a2-45f0-9424-fe9c5722521d

p.10

Mr. Schönharting has served on our board of directors since the Company¡¦s incorporation in July 2005. Mr. Schönharting is a co-founder of the Company. He has also founded or co-founded several other biopharmaceutical companies, including Genmab A/S, Veloxis A/S (f/k/a Life Cycle Pharma A/S), Zealand Pharma A/S and Acadia Pharmaceuticals Inc. Mr. Schönharting has more than 25 years of investment executive experience in public and private equity funds involved in the biopharmaceutical industry. He actively managed BI Healthcare SICAV and BI Bioteknologi SICAV for eight years. Mr. Schönharting currently manages the following funds and certain affiliates of these funds: NB Public Equity K/S, Nordic Biotech K/S, Nordic Biotech Opportunity Fund K/S, NB FP Investment K/S and NB FP Investment II K/S. Mr. Schönharting has an M.Sc. (Econ) from Copenhagen Business School.

Schönharting¥ý¥Í ¦Û¤½¥q©ó 2005 ¦~ 7 ¤ë¦¨¥ß¥H¨Ó¡ASchönharting ¤@ª½¦b§Ú­Ìªº¸³¨Æ·|¥ô¾¡CSchönharting ¥ý¥Í¬O¤½¥qªºÁp¦X³Ð©l¤H¡C ¥LÁٳХߩΦ@¦P³Ð¥ß¤F¨ä¥L´X®a¥Íª«»sÃĤ½¥q¡A¥]¬A Genmab A/S¡BVeloxis A/S¡]f/k/a Life Cycle Pharma A/S¡^¡BZealand Pharma A/S ©M Acadia Pharmaceuticals Inc¡CSchönharting ¥ý¥Í ¦b¯A¤Î¥Íª«»sÃĦæ·~ªº¤½¶Ò©M¨p¶ÒªÑÅv°òª÷¾Ö¦³¶W¹L25¦~ªº§ë¸ê°õ¦æ¸gÅç¡C ¥L¿n·¥ºÞ²z BI Healthcare SICAV ©M BI Bioteknologi SICAV ¤K¦~¡C Schönharting ¥ý¥Í¥Ø«eºÞ²z¥H¤U°òª÷©M³o¨Ç°òª÷ªº¬Y¨ÇÃöÁp¤½¥q¡GNB Public Equity K/S¡BNordic Biotech K/S¡BNordic Biotech Opportunity Fund K/S¡BNB FP Investment K/S ©M NB FP Investment II K/S . Schönharting ¥ý¥Í¾Ö¦³²z¾ÇºÓ¤h¾Ç¦ì¡C (Econ) ¨Ó¦Û­ô¥»«¢®Ú°Ó¾Ç°|¡C

About Forward Pharma

Forward Pharma A/S is a Danish biopharmaceutical company that from 2005 to 2017 developed a proprietary formulation of DMF for the treatment of inflammatory and neurological indications. The Company granted to Biogen an irrevocable license to all of its IP through the License Agreement and received from Biogen a non-refundable cash fee of $1.25 billion in February 2017, with the return of EUR 917.7 million to shareholders through a capital reduction in September 2017.

Ãö©ó Forward Pharma

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---------------

(1)Dermira Announces Positive Topline Results from Phase 2b

GlobeNewswire

www.globenewswire.com › 2019/03/18 › Derm...

Mar 18, 2019 ¡X Dermira Announces Positive Topline Results from Phase 2b Study of

(2)Dermira Prices $130.0 Million Public Offering of Common Stock

March 19, 2019 19:36 ET | Source: Dermira, Inc.

.MENLO PARK, Calif., March 19, 2019 (GLOBE NEWSWIRE) -- Dermira, Inc. (NASDAQ: DERM), a biopharmaceutical company dedicated to bringing biotech ingenuity to medical dermatology by delivering differentiated, new therapies to the millions of patients living with chronic skin conditions, today announced the pricing of its underwritten public offering of 9,811,321 shares of its common stock at a price to the public of $13.25 per share. The gross proceeds to Dermira from the offering, before deducting the underwriting discounts and commissions and estimated offering expenses, are expected to be approximately $130.0 million. In addition, Dermira has granted the underwriters a 30-day option to purchase up to an additional 1,471,698 shares of its common stock, on the same terms and conditions. All of the shares will be offered and sold by Dermira.\\\Lilly Announces Agreement to Acquire Dermira

(3)PR Newswire

www.prnewswire.com › news-releases › lilly-an...

Jan 10, 2020 ¡X (NASDAQ: DERM) today announced a definitive agreement for Lilly to acquire Dermira for $18.75 per share, or approximately $1.1 billion, in an ...

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We are pleased to announce the appointment of Alan Bianchi to the role of Commercial Lead Advisor. Alan is a biopharmaceutical marketing executive with extensive product commercialization and launch experience in dermatology and immunology.

Alan held the role of Head, HCP marketing at Sanofi for the global launches of dupilumab, and most recently, was the Executive Director and US Marketing Lead for the global launches of tralokinumab at LEO Pharma.

Alan will play an important role in the commercial strategy for eblasakimab as we look forward to a topline data readout in early July for the TREK-AD study.

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Connect Biopharma¡¦s Atopic Dermatitis Candidate Shows Rapid, Sustained Improvement Across All Body Regions

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Connect Biopharma Holdings Limited (NASDAQ: CNTB) announced post hoc data analysis from the Phase 2b CBP-201 global trial in moderate-to-severe atopic dermatitis (AD).

The data exhibited that CBP-201 led to rapid and sustained improvement in AD signs and symptoms across all four body regions, compared to the placebo.

EASI subscores improved in all four body regions across 16 weeks of treatment.

Improvements between 300 mg Q2W and Q4W were comparable. At Week 2, EASI decreased by -26.3% (head/neck), -26.4% (trunk), -21.6% (upper limbs), and -23.2% (lower limbs) for patients on CBP-201 300 mg Q4W treatment vs. -9.5% to -15.7% with placebo.

At Week 16, EASI decreased further to -69.2% (head and neck), -72.1% (trunk), -64.2% (upper limbs), and -68.5% (lower limbs) vs. -21.2% to -49.1% with placebo (p<0.01 per region).

Researchers also observed improvement for each classification of AD symptoms (signs): erythema, induration/papulation, lichenification, and excoriation, within each body region.

Concurrently, the company also announced data from Stage 1 of the ongoing pivotal CBP-201 China trial in moderate-to-severe atopic dermatitis (AD), exhibiting rapid relief from symptoms.

The study met primary and secondary endpoints, with mostly mild-to-moderate adverse effects reported.

At 16 weeks, more patients treated with CBP-201 achieved an IGA score of 0-1 (clear or almost clear skin) and a 2-point IGA reduction than those on placebo (30.3% vs. 7.5%).

62.9% of CBP-201 patients achieved a 75% skin clearance (EASI-75), versus 23.4% in the placebo group and EASI-90 of (35.8% vs. 63.%).

Price Action: CNTB shares are up 20.90% at $1.33 during the premarket session on the last check Monday.

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