{"id":878338,"date":"2026-10-11T07:40:18","date_gmt":"2026-10-11T07:40:18","guid":{"rendered":"https:\/\/www.newsbeep.com\/us\/878338\/"},"modified":"2026-10-11T07:40:18","modified_gmt":"2026-10-11T07:40:18","slug":"fda-review-docs-spark-revolution-sell-off-zealand-diabetes-data-underwhelm-analysts","status":"publish","type":"post","link":"https:\/\/www.newsbeep.com\/us\/878338\/","title":{"rendered":"FDA review docs spark Revolution sell-off; Zealand diabetes data underwhelm analysts"},"content":{"rendered":"\n<p class=\"text text-block paragraph text-left neo-font-paragraph-xl-reg  yf-18d6y07\" style=\"text-decoration: none; font-style: normal; text-transform: none; text-align: inherit; font-variant-numeric: normal;\">This story was originally published on BioPharma Dive. To receive daily news and insights, subscribe to our free daily <a href=\"https:\/\/www.biopharmadive.com\/signup\/?utm_campaign=Yahoo-Licensed-Content&amp;utm_source=yahoo&amp;utm_medium=referral\" data-ylk=\"slk:BioPharma%20Dive%20newsletter;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;BioPharma Dive newsletter&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">BioPharma Dive newsletter<\/a>.  <\/p>\n<p class=\"text text-block paragraph text-left neo-font-paragraph-xl-reg  yf-18d6y07\" style=\"text-decoration: none; font-style: normal; text-transform: none; text-align: inherit; font-variant-numeric: normal;\">Today, a brief rundown of news involving Revolution Medicines and Zealand Pharma, as well as updates from Pfizer, Ultragenyx and TCGX that you may have missed.  <\/p>\n<p class=\"text text-block paragraph text-left neo-font-paragraph-xl-reg  yf-18d6y07\" style=\"text-decoration: none; font-style: normal; text-transform: none; text-align: inherit; font-variant-numeric: normal;\">Shares of Revolution Medicine fell 6% Thursday following release of <a href=\"https:\/\/www.accessdata.fda.gov\/drugsatfda_docs\/nda\/2026\/220910Orig1s000MultidisciplineR.pdf\" data-ylk=\"slk:Food%20and%20Drug%20Administration;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;Food and Drug Administration&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">Food and Drug Administration<\/a><a href=\"https:\/\/www.accessdata.fda.gov\/drugsatfda_docs\/nda\/2026\/220910Orig1s000MultidisciplineR.pdf\" data-ylk=\"slk:review%20documents;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;review documents&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\"> review documents<\/a> suggesting the company&#8217;s closely watched pancreatic cancer drug Rasonque might be less effective in certain patients for which it&#8217;s approved. Rasonque <a href=\"https:\/\/www.biopharmadive.com\/news\/revolution-daraxonrasib-rasonque-approval-fda-priority-review-voucher\/828847\/\" data-ylk=\"slk:gained%20FDA%20approval;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;gained FDA approval&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">gained FDA approval<\/a> in August based on data showing it <a href=\"https:\/\/www.biopharmadive.com\/news\/revolution-daraxonrasib-asco-2026-rasolute-study-results\/821555\/\" data-ylk=\"slk:nearly%20doubled%20survival;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;nearly doubled survival&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">nearly doubled survival<\/a> compared to chemotherapy in patients who&#8217;d already progressed on chemo. However, the FDA documents showed that tumor responses were markedly better than chemo in trial enrollees with a specific KRAS mutation called G12V. The difference was more modest among those with a &#8220;G12D&#8221; mutation \u2014 who represent the largest share of pancreatic cancer patients \u2014 and worse in people with a &#8220;G12R&#8221; mutation. Many Wall Street analysts rushed to Revolution&#8217;s defense, arguing in client notes that the sell-off was &#8220;overdone,&#8221; &#8220;misguided&#8221; or an investor &#8220;overreaction.&#8221; Still, Leerink Partners analyst Andrew Berens referred to the disclosure as a &#8220;crack in the armor&#8221; for Rasonque and viewed it as an opportunity for competitors with G12D-specific inhibitors or next-generation medicines. \u2014 Jonathan Gardner  <\/p>\n<p class=\"text text-block paragraph text-left neo-font-paragraph-xl-reg  yf-18d6y07\" style=\"text-decoration: none; font-style: normal; text-transform: none; text-align: inherit; font-variant-numeric: normal;\">Zealand Pharma said Wednesday its experimental, Roche-partnered drug petrelintide helped people with obesity and diabetes in a Phase 2 trial <a href=\"http:\/\/www.globenewswire.com\/news-release\/2026\/10\/07\/3376750\/0\/en\/zealand-pharma-announces-positive-phase-2-zupreme-2-topline-results-for-amylin-analog-petrelintide-in-people-with-overweight-or-obesity-and-type-2-diabetes.html\" data-ylk=\"slk:lose%20up%20to%209%25%20of%20their%20body%20weight;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;lose up to 9% of their body weight&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">lose up to 9% of their body weight<\/a> over 28 weeks, equating to 7 percentage points more than those who got a placebo. Petrelintide was also associated with &#8220;clinically relevant&#8221; blood sugar reductions that were anywhere from about 0.6 to 0.9 percentage points better than a placebo. Multiple Wall Street analysts noted that weight loss numbers were comparable to an Eli Lilly drug that, like petrelintide, is an &#8220;amylin analog&#8221; and a potential alternative to GLP-1 medicines. They also applauded the therapy&#8217;s seemingly &#8220;benign&#8221; safety profile. Petrelintide&#8217;s effects on blood sugar, though, were viewed as less impressive. The drug will &#8220;likely be used primarily in the maintenance setting,&#8221; William Blair analyst Andy Hsieh predicted in a client note. \u2014 Jonathan Gardner  <\/p>\n<p class=\"text text-block paragraph text-left neo-font-paragraph-xl-reg  yf-18d6y07\" style=\"text-decoration: none; font-style: normal; text-transform: none; text-align: inherit; font-variant-numeric: normal;\">The FDA has <a href=\"https:\/\/investors.pfizer.com\/Investors\/news-events\/News\/news-details\/2026\/Pfizers-TUKYSA-Regimen-Receives-FDA-Approval-as-Front-Line-Maintenance-Treatment-for-HER2-Metastatic-Breast-Cancer\/default.aspx\" data-ylk=\"slk:expanded%20use;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;expanded use&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">expanded use<\/a> of Pfizer&#8217;s HER2-targeting breast cancer drug Tukysa. Previously developed by Seagen, Tukysa <a href=\"https:\/\/www.biopharmadive.com\/news\/seattle-genetics-fda-approval-breast-cancer-tucatinib\/576311\/\" data-ylk=\"slk:first%20came%20to%20market%20in%202020;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;first came to market in 2020&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">first came to market in 2020<\/a> as a second-line treatment for HER2-positive breast tumors. The new clearance makes Tukysa available in the frontline setting, where it&#8217;ll be prescribed as part of a &#8220;chemotherapy-free maintenance&#8221; regimen also involving the targeted medications Herceptin and Perjeta. That regimen was associated with a 36% reduction in the risk of disease progression or death when compared to Herceptin and Perjeta alone in a Phase 3 trial. \u2014 Delilah Alvarado  <\/p>\n<p class=\"text text-block paragraph text-left neo-font-paragraph-xl-reg  yf-18d6y07\" style=\"text-decoration: none; font-style: normal; text-transform: none; text-align: inherit; font-variant-numeric: normal;\">Ultragenyx has <a href=\"https:\/\/ir.ultragenyx.com\/news-releases\/news-release-details\/ultragenyx-enters-agreement-sell-rare-pediatric-disease-priority\" data-ylk=\"slk:gained%20%24210%20million;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;gained $210 million&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">gained $210 million<\/a> by selling one of two regulatory fast passes it was recently awarded by the FDA. The priority voucher Ultragenyx sold on Wednesday was related <a href=\"http:\/\/www.biopharmadive.com\/news\/ultragenyx-fda-approve-genglycos-GSDIa-gene-therapy\/828369\/\" data-ylk=\"slk:to%20the%20clearance%20of;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;to the clearance of&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">to the clearance of <\/a><a href=\"http:\/\/www.biopharmadive.com\/news\/ultragenyx-fda-approve-genglycos-GSDIa-gene-therapy\/828369\/\" data-ylk=\"slk:Glenglycos;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;Glenglycos&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">Glenglycos<\/a>, a gene therapy for a rare glycogen storage disease. It received another upon the approval of the <a href=\"https:\/\/www.biopharmadive.com\/news\/ultragenyx-fayuvi-orum-bristol-lunsumio-longeveron-rocket-danon\/830512\/\" data-ylk=\"slk:Sanfilippo%20gene%20therapy;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;Sanfilippo gene therapy&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">Sanfilippo gene therapy <\/a><a href=\"https:\/\/www.biopharmadive.com\/news\/ultragenyx-fayuvi-orum-bristol-lunsumio-longeveron-rocket-danon\/830512\/\" data-ylk=\"slk:Fayuvi;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;Fayuvi&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">Fayuvi<\/a><a href=\"https:\/\/www.biopharmadive.com\/news\/ultragenyx-fayuvi-orum-bristol-lunsumio-longeveron-rocket-danon\/830512\/\" data-ylk=\"slk:.;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;.&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">.<\/a> The sale is an &#8220;incrementally positive&#8221; development for Ultragenyx, as it&#8217;ll &#8220;significantly&#8221; strengthen the company&#8217;s balance sheet, wrote William Blair analyst Lachlan Hanbury-Brown. The company said it would <a href=\"https:\/\/www.biopharmadive.com\/news\/ultragenyx-angelman-syndrome-drug-results-cost-cuts\/829528\/\" data-ylk=\"slk:consider%20cost%20cuts;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;consider cost cuts&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">consider cost cuts<\/a> last month following the failure of a key experimental treatment for Angelman syndrome. \u2014 Delilah Alvarado  <\/p>\n<p class=\"text text-block paragraph text-left neo-font-paragraph-xl-reg  yf-18d6y07\" style=\"text-decoration: none; font-style: normal; text-transform: none; text-align: inherit; font-variant-numeric: normal;\">Biotech investment firm TCGX said <a href=\"https:\/\/www.businesswire.com\/news\/home\/20261007924776\/en\/TCGX-Announces-Oversubscribed-%24600-Million-Asia-Fund\" data-ylk=\"slk:Wednesday%20it%20closed%20a%20%24600%20million%20fund;elm:context_link;itc:0;sec:content-canvas;source:content-canvas%20default\" data-yga=\"{&quot;yLinkText&quot;:&quot;Wednesday it closed a $600 million fund&quot;,&quot;yLinkElement&quot;:&quot;context_link&quot;,&quot;yModuleName&quot;:&quot;content-canvas&quot;,&quot;yTrafficOrigin&quot;:&quot;content-canvas default&quot;}\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">Wednesday it closed a $600 million fund<\/a> that will support biotechnology companies in Asia. Known as TCGX Asia Life Sciences Fund I, the investment vehicle will operate separately from, but in &#8220;close synergy&#8221; with, two other TCGX funds that back biotechs in the U.S. and Europe. It is backed by a &#8220;diverse group of international institutional investors,&#8221; said TCGX, without providing specifics. The firm is opening new offices in Shanghai and Hong Kong alongside the fund&#8217;s launch. \u2014 Delilah Alvarado  <\/p>\n<p class=\"text text-block paragraph text-left neo-font-paragraph-xl-reg  yf-18d6y07\" style=\"text-decoration: none; font-style: normal; text-transform: none; text-align: inherit; font-variant-numeric: normal;\">Recommended Reading  <\/p>\n","protected":false},"excerpt":{"rendered":"This story was originally published on BioPharma Dive. To receive daily news and insights, subscribe to our free&hellip;\n","protected":false},"author":2,"featured_media":878339,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[58],"tags":[5097,28,122,101,939,2993,97,2994,32455,2995,932,243,32456,20112,147,9323,1170,1666,6480,2996,2997,923,19533,3733,32457],"class_list":["post-878338","post","type-post","status-publish","format-standard","has-post-thumbnail","category-medication","tag-401k","tag-business","tag-business-news","tag-economy","tag-finance","tag-financial-information","tag-health","tag-investing","tag-investment-tools","tag-investor","tag-market-news","tag-medication","tag-mortgage","tag-mutual-funds","tag-personal-finance","tag-quote","tag-real-estate","tag-retirement","tag-stock","tag-stock-research","tag-stock-valuation","tag-stocks","tag-suze-orman","tag-tax","tag-track-portfolio"],"_links":{"self":[{"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/posts\/878338","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/comments?post=878338"}],"version-history":[{"count":0,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/posts\/878338\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/media\/878339"}],"wp:attachment":[{"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/media?parent=878338"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/categories?post=878338"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/tags?post=878338"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}