<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0" xmlns:media="http://search.yahoo.com/mrss/">
  <channel>
    <title>Genitourinary/sexual function</title>
    <description>
      <![CDATA[]]>
    </description>
    <link>https://www.bioworld.com/rss</link>
    <language>en-us</language>
    <item>
      <title>Travere expands rare kidney portfolio in $1B+ Everest deal </title>
      <description>
        <![CDATA[Less than two months after winning FDA approval for a second indication for Filspari (sparsentan), Travere Therapeutics Inc. added to its rare kidney disease pipeline by exclusively licensing civorebrutinib from Everest Medicines Ltd. in a deal that could be worth more than $1.14 billion.]]>
      </description>
      <guid>http://www.bioworld.com/articles/731526</guid>
      <pubDate>Tue, 02 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731526-travere-expands-rare-kidney-portfolio-in-1b-everest-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Nephrology-Renal-Kidney.webp?t=1669825127" type="image/png" medium="image" fileSize="946164">
        <media:title type="plain">3D illustration of kidney cross section</media:title>
      </media:content>
    </item>
    <item>
      <title>Sun Pharma to acquire Merck spinoff Organon for $11.75B</title>
      <description>
        <![CDATA[Sun Pharmaceuticals Industries Ltd. will pay $11.75 billion cash to acquire Organon & Co. The transaction is expected to close in early 2027. The addition of Organon’s women’s health products, legacy drug brands and biosimilars are expected to boost Mumbai, India-based Sun’s global reach. The all-cash buy is also expected to relieve Jersey City, N.J.-based Organon of an $8.6 billion debt pile, accumulated after its debt-laden 2021 spinout from Merck & Co. Inc.]]>
      </description>
      <guid>http://www.bioworld.com/articles/730787</guid>
      <pubDate>Tue, 28 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730787-sun-pharma-to-acquire-merck-spinoff-organon-for-1175b</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Three-red-darts-on-target.webp?t=1761844421" type="image/jpeg" medium="image" fileSize="465362">
        <media:title type="plain">Three red darts on target</media:title>
      </media:content>
    </item>
    <item>
      <title>Sun Pharma to acquire Merck spinoff Organon for $11.75B</title>
      <description>
        <![CDATA[Sun Pharmaceuticals Industries Ltd. will pay $11.75 billion cash to acquire Organon & Co. The transaction is expected to close in early 2027. The addition of Organon’s women’s health products, legacy drug brands and biosimilars are expected to boost Mumbai, India-based Sun’s global reach. The all-cash buy is also expected to relieve Jersey City, N.J.-based Organon of an $8.6 billion debt pile, accumulated after its debt-laden 2021 spinout from Merck & Co. Inc.]]>
      </description>
      <guid>http://www.bioworld.com/articles/730643</guid>
      <pubDate>Mon, 27 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730643-sun-pharma-to-acquire-merck-spinoff-organon-for-1175b</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Three-red-darts-on-target.webp?t=1761844421" type="image/jpeg" medium="image" fileSize="465362">
        <media:title type="plain">Three red darts on target</media:title>
      </media:content>
    </item>
    <item>
      <title>Xeltis secures CE mark for Axess, its hemodialysis conduit</title>
      <description>
        <![CDATA[Xeltis BV has secured CE mark approval for Axess, its restorative vascular access conduit for hemodialysis. The company also released 12-month data from its EU pivotal trial on the technology, which showed strong durability outcomes, including 79% secondary patency and a very low patency‑related reintervention rate of 1.3 per patient-year, as well as a substantial reduction in infection burden.]]>
      </description>
      <guid>http://www.bioworld.com/articles/730483</guid>
      <pubDate>Tue, 21 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730483-xeltis-secures-ce-mark-for-axess-its-hemodialysis-conduit</link>
      <media:content url="https://www.bioworld.com/ext/resources/2025/Xeltis-Axess-vascular-access-conduit-8jan25jpg.webp?t=1776800189" type="image/jpeg" medium="image" fileSize="34193">
        <media:title type="plain">Xeltis-Axess-vascular-access-conduit-8jan25jpg.jpg</media:title>
        <media:description type="plain">Axess vascular access conduit. Credit: Xeltis BV</media:description>
      </media:content>
    </item>
    <item>
      <title>Travere’s Filspari approved for rare kidney disease FSGS</title>
      <description>
        <![CDATA[Becoming the first and only fully FDA-approved treatment for focal segmental glomerulosclerosis (FSGS), Travere Therapeutics Inc.’s Filspari (sparsentan) has gained access to a second lucrative market with a regulatory package that validates proteinuria as a surrogate endpoint.]]>
      </description>
      <guid>http://www.bioworld.com/articles/730293</guid>
      <pubDate>Tue, 14 Apr 2026 08:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730293-traveres-filspari-approved-for-rare-kidney-disease-fsgs</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidneys-pills-and-chart-line.webp?t=1762551836" type="image/jpeg" medium="image" fileSize="432770">
        <media:title type="plain">Kidneys, pills and chart line</media:title>
      </media:content>
    </item>
    <item>
      <title>Highly complementary Biogen pays $5.6B; who’s jealous of Apellis? </title>
      <description>
        <![CDATA[Biogen Inc. hardly blinked at the competition faced by Apellis Pharmaceuticals Inc. as the two companies sealed a deal whereby the former has agreed to acquire all outstanding shares of the latter for $41 each, or about $5.6 billion.]]>
      </description>
      <guid>http://www.bioworld.com/articles/729963</guid>
      <pubDate>Tue, 31 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729963-highly-complementary-biogen-pays-56b-whos-jealous-of-apellis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Handshake-with-charts-maps-data.webp?t=1701801114" type="image/jpeg" medium="image" fileSize="281005">
        <media:title type="plain">Handshake with charts, maps, data</media:title>
      </media:content>
    </item>
    <item>
      <title>PKU ballyhoo averting Street’s gaze from Maze phase II AMKD win?</title>
      <description>
        <![CDATA[Maze Therapeutics Inc. continues its journey toward a pivotal program after sharing positive top-line data from the phase II Horizon study with MZE-829, an oral, small-molecule, dual-mechanism APOL1 inhibitor, in patients with broad APOL1-mediated kidney disease (AMKD).]]>
      </description>
      <guid>http://www.bioworld.com/articles/729839</guid>
      <pubDate>Wed, 25 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729839-pku-ballyhoo-averting-streets-gaze-from-maze-phase-ii-amkd-win</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidney-disease-illustration.webp?t=1599165012" type="image/png" medium="image" fileSize="370906">
        <media:title type="plain">Kidney disease illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Kintor’s KX-826 meets phase III endpoints in alopecia  </title>
      <description>
        <![CDATA[Kintor Pharmaceutical Ltd.’s topical androgen receptor antagonist, pyrilutamide (KX-826), met the primary endpoint in a pivotal phase III trial in male androgenetic alopecia, and the company will soon file an NDA with China’s National Medical Products Administration.]]>
      </description>
      <guid>http://www.bioworld.com/articles/729893</guid>
      <pubDate>Tue, 24 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729893-kintors-kx-826-meets-phase-iii-endpoints-in-alopecia</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Dermatologic/Alopecia.webp?t=1773953185" type="image/jpeg" medium="image" fileSize="1021257">
        <media:title type="plain">Alopecia - hair loss </media:title>
      </media:content>
    </item>
    <item>
      <title>Kintor’s KX-826 meets phase III endpoints in alopecia  </title>
      <description>
        <![CDATA[Kintor Pharmaceutical Ltd.’s topical androgen receptor antagonist, pyrilutamide (KX-826), met the primary endpoint in a pivotal phase III trial in male androgenetic alopecia, and the company will soon file an NDA with China’s National Medical Products Administration.]]>
      </description>
      <guid>http://www.bioworld.com/articles/729749</guid>
      <pubDate>Thu, 19 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729749-kintors-kx-826-meets-phase-iii-endpoints-in-alopecia</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Dermatologic/Alopecia.webp?t=1773953185" type="image/jpeg" medium="image" fileSize="1021257">
        <media:title type="plain">Alopecia - hair loss </media:title>
      </media:content>
    </item>
    <item>
      <title>China approves first noninvasive therapy for cervical precancer</title>
      <description>
        <![CDATA[China’s National Medical Products Administration has approved Asieris Pharmaceuticals Co. Ltd.’s cold light photodynamic drug-device combination product, Cevira (APL-1702, hexaminolevulinate hydrochloride), which is used as a nonsurgical therapy for treating patients with cervical intraepithelial neoplasia grade 2.]]>
      </description>
      <guid>http://www.bioworld.com/articles/729585</guid>
      <pubDate>Tue, 10 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729585-china-approves-first-noninvasive-therapy-for-cervical-precancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Sexual-health/women-gyno-uterus-ovary.webp?t=1589293258" type="image/png" medium="image" fileSize="483965">
        <media:title type="plain">Fallopian tubes, ovaries and uterus</media:title>
      </media:content>
    </item>
    <item>
      <title>Vertex filing BLA for ‘best-in-class’ IgAN drug on Rainier win</title>
      <description>
        <![CDATA[Vertex Pharmaceuticals Inc. is on track to complete a BLA by the end of March seeking potential U.S. accelerated approval for povetacicept, its dual inhibitor of the BAFF and APRIL cytokines, to treat immunoglobulin A nephropathy (IgAN), following a successful phase III Rainier trial.]]>
      </description>
      <guid>http://www.bioworld.com/articles/729449</guid>
      <pubDate>Tue, 10 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729449-vertex-filing-bla-for-best-in-class-igan-drug-on-rainier-win</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidneys.webp?t=1585681893" type="image/png" medium="image" fileSize="393213">
        <media:title type="plain">Kidneys</media:title>
      </media:content>
    </item>
    <item>
      <title>China approves first noninvasive therapy for cervical precancer</title>
      <description>
        <![CDATA[China’s National Medical Products Administration has approved Asieris Pharmaceuticals Co. Ltd.’s cold light photodynamic drug-device combination product, Cevira (APL-1702, hexaminolevulinate hydrochloride), which is used as a nonsurgical therapy for treating patients with cervical intraepithelial neoplasia grade 2.]]>
      </description>
      <guid>http://www.bioworld.com/articles/729303</guid>
      <pubDate>Wed, 04 Mar 2026 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/729303-china-approves-first-noninvasive-therapy-for-cervical-precancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Sexual-health/women-gyno-uterus-ovary.webp?t=1589293258" type="image/png" medium="image" fileSize="483965">
        <media:title type="plain">Fallopian tubes, ovaries and uterus</media:title>
      </media:content>
    </item>
    <item>
      <title>Innovacell’s $91M Tokyo IPO to fund incontinence cell therapies </title>
      <description>
        <![CDATA[Innovacell Inc. launched a ¥14.16 billion (US$91.2 million) stock sale on the Tokyo Stock Exchange Feb. 24, ending a near two-year lull of biotech listings in Japan while signaling a dynamic year ahead for cell-based therapeutics.]]>
      </description>
      <guid>http://www.bioworld.com/articles/729194</guid>
      <pubDate>Tue, 24 Feb 2026 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/729194-innovacells-91m-tokyo-ipo-to-fund-incontinence-cell-therapies</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Glass-yen-yuan-symbol.webp?t=1664308599" type="image/png" medium="image" fileSize="289038">
        <media:title type="plain">Glass yen/yuan symbol</media:title>
      </media:content>
    </item>
    <item>
      <title>Otsuka’s IgAN therapy gets a thumbs-up from the FDA</title>
      <description>
        <![CDATA[The priority BLA from Otsuka Pharmaceutical Co. Ltd., of Tokyo, and its U.S. subsidiary, Otsuka Pharmaceutical Development & Commercialization Inc., for sibeprenlimab to treat immunoglobulin A nephropathy (IgAN) has received accelerated approved by the U.S. FDA.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726792</guid>
      <pubDate>Tue, 02 Dec 2025 00:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726792-otsukas-igan-therapy-gets-a-thumbs-up-from-the-fda</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidneys2.webp?t=1637092651" type="image/png" medium="image" fileSize="254506">
        <media:title type="plain">Kidneys</media:title>
      </media:content>
    </item>
    <item>
      <title>Otsuka’s IgAN therapy gets a thumbs-up from the FDA</title>
      <description>
        <![CDATA[The priority BLA from Otsuka Pharmaceutical Co. Ltd., of Tokyo, and its U.S. subsidiary, Otsuka Pharmaceutical Development & Commercialization Inc., for sibeprenlimab to treat immunoglobulin A nephropathy (IgAN) has received accelerated approved by the U.S. FDA.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726713</guid>
      <pubDate>Wed, 26 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726713-otsukas-igan-therapy-gets-a-thumbs-up-from-the-fda</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidneys2.webp?t=1637092651" type="image/png" medium="image" fileSize="254506">
        <media:title type="plain">Kidneys</media:title>
      </media:content>
    </item>
    <item>
      <title>Qilu gains China rights to Laekna’s AKT inhibitor in ¥2B deal</title>
      <description>
        <![CDATA[Laekna Inc. outlicensed select rights to LAE-002 (afuresertib), an oral pan-AKT kinase inhibitor licensed from Novartis AG in 2018, to Qilu Pharmaceutical Co. Ltd. under a potential ¥2.045 billion (US$287.23 million) deal.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726370</guid>
      <pubDate>Tue, 18 Nov 2025 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726370-qilu-gains-china-rights-to-laeknas-akt-inhibitor-in-2b-deal</link>
    </item>
    <item>
      <title>Qilu gains China rights to Laekna’s AKT inhibitor in ¥2B deal</title>
      <description>
        <![CDATA[Laekna Inc. outlicensed select rights to LAE-002 (afuresertib), an oral pan-AKT kinase inhibitor licensed from Novartis AG in 2018, to Qilu Pharmaceutical Co. Ltd. under a potential ¥2.045 billion (US$287.23 million) deal.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726126</guid>
      <pubDate>Wed, 12 Nov 2025 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726126-qilu-gains-china-rights-to-laeknas-akt-inhibitor-in-2b-deal</link>
    </item>
    <item>
      <title>Up the bladder ladder, Engene tweak means phase II bell rung</title>
      <description>
        <![CDATA[Engene Holdings Inc.’s protocol amendment to its phase II trial with detalimogene voraplasmid in bladder cancer worked out in a big way, and shares of the firm closed Nov. 11 at $8.82, up $2.81, or 47%. Engene rolled out additional preliminary data from the pivotal cohort of the ongoing Legend study testing the nonviral gene therapy in high-risk, Bacillus Calmette-Guérin-unresponsive non-muscle invasive bladder cancer with carcinoma in situ, with or without concomitant papillary disease.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726109</guid>
      <pubDate>Tue, 11 Nov 2025 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726109-up-the-bladder-ladder-engene-tweak-means-phase-ii-bell-rung</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Urology/Art-concept-for-bladder.webp?t=1733435225" type="image/jpeg" medium="image" fileSize="250443">
        <media:title type="plain">Art concept for bladder</media:title>
      </media:content>
    </item>
    <item>
      <title>Abortion dispute active, FDA clears new generic pill </title>
      <description>
        <![CDATA[With U.S. President Donald Trump’s administration vocally opposed to abortion, the U.S. FDA has approved a new generic version of the pill that makes the procedure possible medically: mifepristone, once better known as RU-486.]]>
      </description>
      <guid>http://www.bioworld.com/articles/724728</guid>
      <pubDate>Fri, 03 Oct 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/724728-abortion-dispute-active-fda-clears-new-generic-pill</link>
    </item>
    <item>
      <title>CHMP recommends EU approval of Bayer’s Lynkuet for hot flashes</title>
      <description>
        <![CDATA[Following the first approvals in the U.K., Canada, Australia and Switzerland, the EMA’s Committee for Medicinal Products for Human Use (CHMP) is now recommending approval of Bayer AG’s Lynkuet (elinzanetant), a non-hormonal treatment for symptoms of menopause. The drug, the first dual neurokinin-1 and neurokinin-3 receptor antagonist, is for the treatment of moderate to severe vasomotor symptoms, also known as hot flashes.]]>
      </description>
      <guid>http://www.bioworld.com/articles/724310</guid>
      <pubDate>Fri, 19 Sep 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/724310-chmp-recommends-eu-approval-of-bayers-lynkuet-for-hot-flashes</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Person-holding-pills-and-glass-of-water.webp?t=1744924970" type="image/jpeg" medium="image" fileSize="128864">
        <media:title type="plain">Person holding pills and glass of water</media:title>
      </media:content>
    </item>
    <item>
      <title>Wall Street solutes phase I data from Maze in CKD, PKU</title>
      <description>
        <![CDATA[Maze Therapeutics Inc. CEO Jason Coloma said the latest phase I results with MZE-782, a prospect for phenylketonuria (PKU) as well as chronic kidney disease (CKD), bolster the firm’s “conviction to move into phase II” next year in both indications.]]>
      </description>
      <guid>http://www.bioworld.com/articles/724058</guid>
      <pubDate>Thu, 11 Sep 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/724058-wall-street-solutes-phase-i-data-from-maze-in-ckd-pku</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Clinics/Clinical-data-illustration.webp?t=1621541773" type="image/png" medium="image" fileSize="381492">
        <media:title type="plain">Clinical data illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Vor and Remegen post another phase III win</title>
      <description>
        <![CDATA[The recombinant fusion protein drug telitacicept from Remegen Co. Ltd. and Vor Bio Inc. has notched a phase III win in treating adults with IgA nephropathy. The clinical trial of the fusion protein hit the primary endpoint, reducing proteinuria, too much protein in patients’ urine, in stage A of the study in China.]]>
      </description>
      <guid>http://www.bioworld.com/articles/723861</guid>
      <pubDate>Tue, 02 Sep 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/723861-vor-and-remegen-post-another-phase-iii-win</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidney-disease-illustration.webp?t=1599165012" type="image/png" medium="image" fileSize="370906">
        <media:title type="plain">Kidney disease illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Vor and Remegen post another phase III win</title>
      <description>
        <![CDATA[The recombinant fusion protein drug telitacicept from Remegen Co. Ltd. and Vor Bio Inc. has notched a phase III win in treating adults with IgA nephropathy. The clinical trial of the fusion protein hit the primary endpoint, reducing proteinuria, too much protein in patients’ urine, in stage A of the study in China.]]>
      </description>
      <guid>http://www.bioworld.com/articles/723327</guid>
      <pubDate>Wed, 27 Aug 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/723327-vor-and-remegen-post-another-phase-iii-win</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidney-disease-illustration.webp?t=1599165012" type="image/png" medium="image" fileSize="370906">
        <media:title type="plain">Kidney disease illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Apellis’ Empaveli approved in US for two rare kidney diseases</title>
      <description>
        <![CDATA[Following a priority review, Apellis Pharmaceuticals Inc. received U.S. FDA approval of a supplemental NDA making pegcetacoplan the second marketed treatment for complement 3 glomerulopathy and the first for primary immune complex membranoproliferative glomerulonephritis.]]>
      </description>
      <guid>http://www.bioworld.com/articles/722735</guid>
      <pubDate>Tue, 29 Jul 2025 15:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/722735-apellis-empaveli-approved-in-us-for-two-rare-kidney-diseases</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Empaveli-7-29.webp?t=1753822733" type="image/png" medium="image" fileSize="159592">
        <media:title type="plain">Empaveli</media:title>
        <media:description type="plain">Credit: Apellis Pharmaceuticals Inc.</media:description>
      </media:content>
    </item>
    <item>
      <title>Kintor’s KX-826 meets phase II endpoints in male alopecia </title>
      <description>
        <![CDATA[Suzhou, China-based Kintor Pharmaceutical Ltd.’s KX-826 met the primary endpoint in a phase II trial for treating male adult androgenetic alopecia (AGA). Kintor is developing KX-826 (pyrilutamide), an androgen receptor inhibitor, for topical treatment of AGA as well as acne vulgaris.]]>
      </description>
      <guid>http://www.bioworld.com/articles/722711</guid>
      <pubDate>Tue, 29 Jul 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/722711-kintors-kx-826-meets-phase-ii-endpoints-in-male-alopecia</link>
    </item>
    <item>
      <title>Kintor’s KX-826 meets phase II endpoints in male alopecia </title>
      <description>
        <![CDATA[Suzhou, China-based Kintor Pharmaceutical Ltd.’s KX-826 met the primary endpoint in a phase II trial for treating male adult androgenetic alopecia (AGA). Kintor is developing KX-826 (pyrilutamide), an androgen receptor inhibitor, for topical treatment of AGA as well as acne vulgaris.]]>
      </description>
      <guid>http://www.bioworld.com/articles/722423</guid>
      <pubDate>Thu, 24 Jul 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/722423-kintors-kx-826-meets-phase-ii-endpoints-in-male-alopecia</link>
    </item>
    <item>
      <title>Renasant launches with $54.5M to develop drugs for a genetic kidney disease</title>
      <description>
        <![CDATA[Launched out of 5AM Ventures’ 4:59 Initiative, Renasant Bio Inc. has secured $54.5 million in seed funding to support development of treatments for autosomal dominant polycystic kidney disease (ADPKD), a genetic disease caused by mutations in the PKD1 and PKD2 genes, which encode polycystin proteins PC1 and PC2 that come together to form a calcium ion channel vital for kidney function.]]>
      </description>
      <guid>http://www.bioworld.com/articles/722151</guid>
      <pubDate>Tue, 15 Jul 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/722151-renasant-launches-with-545m-to-develop-drugs-for-a-genetic-kidney-disease</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/kidney-genetic-congenital.webp?t=1709655526" type="image/jpeg" medium="image" fileSize="168177">
        <media:title type="plain">Illustration of kidney with DNA structures</media:title>
      </media:content>
    </item>
    <item>
      <title>Prokidney produces positive phase II CKD data, thunderous stock surge</title>
      <description>
        <![CDATA[A mixed bag of top-line phase II data prompted stellar stock results for Prokidney Corp. and its chronic kidney disease (CKD) and diabetes therapy, rilparencel. The results came from two arms of the study, each with its own treatment regime. The market heartily took to the results as the company’s stock (NASDAQ:PROK) closed 515% upward at $3.73 per share after starting the day under $1 each.]]>
      </description>
      <guid>http://www.bioworld.com/articles/721910</guid>
      <pubDate>Tue, 08 Jul 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721910-prokidney-produces-positive-phase-ii-ckd-data-thunderous-stock-surge</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidney-disease-illustration.webp?t=1599165012" type="image/png" medium="image" fileSize="370906">
        <media:title type="plain">Kidney disease illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Jyong’s $20M US IPO to help refile NDA of urological botanic drug</title>
      <description>
        <![CDATA[Jyong Biotech Ltd. raised $20 million from its Nasdaq debut June 17 to advance a pipeline of botanical drugs targeting male urinary disorders. The New Taipei City, Taiwan-headquartered company’s shares began trading under the ticker MENS, and closed at $10.11 apiece at the bell, up 34.80% from its listing price of $7.50 per share. Shares had kicked up to $15 at opening, reaching double its offering price.]]>
      </description>
      <guid>http://www.bioworld.com/articles/721538</guid>
      <pubDate>Tue, 24 Jun 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721538-jyongs-20m-us-ipo-to-help-refile-nda-of-urological-botanic-drug</link>
    </item>
    <item>
      <title>Jyong’s $20M US IPO to help refile NDA of urological botanic drug</title>
      <description>
        <![CDATA[Jyong Biotech Ltd. raised $20 million from its Nasdaq debut June 17 to advance a pipeline of botanical drugs targeting male urinary disorders. The New Taipei City, Taiwan-headquartered company’s shares began trading under the ticker MENS, and closed at $10.11 apiece at the bell, up 34.80% from its listing price of $7.50 per share. Shares had kicked up to $15 at opening, reaching double its offering price.]]>
      </description>
      <guid>http://www.bioworld.com/articles/721456</guid>
      <pubDate>Wed, 18 Jun 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721456-jyongs-20m-us-ipo-to-help-refile-nda-of-urological-botanic-drug</link>
    </item>
  </channel>
</rss>
