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			<title>365 Injections a Year, or 52. A New FDA Approval Gives Families With Achondroplasia a Meaningful Choice.</title>
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			<title>At a Moment When Federal Cancer Funding Is Being Cut Sharply, the ACS Just Invested in the Next Generation of Researchers. Here’s What That Means.</title>
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			<title>The FDA Just Rewrote the Hormone Therapy Label. Twenty-Three Years After a Study Scared Women Away From Treatment, Here’s What Actually Changed — and What Didn’t.</title>
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			<title>Foundayo Was Approved in 50 Days. Now the FDA Wants a Decade of Safety Follow-Up. Here’s What’s Actually Being Studied — and Why.</title>
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			<title>A Rare Cancer With No Good Options Gets a New Investigational Path. What the FDA’s Orphan Drug Designation for Eftilagimod Alfa Actually Signals.</title>
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			<title>Confirmation</title>
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			<title>The Number One Reason Parents Don’t Use Epinephrine in Time Is Fear of the Needle. neffy® Just Got Cleared for More Young Children.</title>
			<pubDate><![CDATA[Sat, 25 Apr 2026 19:23:22 +0000]]></pubDate>
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			<title>Younger Endometrial Cancer Survivors Face Years of Unnecessary Suffering. New Evidence Says One Treatment Has Been Wrongly Withheld.</title>
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			<link><![CDATA[https://healthevidencedigest.com/fda-accepts-ultragenyxs-resubmitted-bla-for-ux111-gene-therapy-in-sanfilippo-syndrome-type-a/]]></link>
			<title>Eight Years, No Treatment. The UX111 Sanfilippo Gene Therapy Is Now One Step From Approval — and the Data Behind It Is Remarkable.</title>
			<pubDate><![CDATA[Sat, 25 Apr 2026 18:46:48 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/hormone-therapy-underused-in-women-with-premature-ovarian-insufficiency-in-menopause/]]></guid>
			<link><![CDATA[https://healthevidencedigest.com/hormone-therapy-underused-in-women-with-premature-ovarian-insufficiency-in-menopause/]]></link>
			<title>She’s 28 and in Menopause. Two-Thirds of Women Like Her Aren’t Getting the Treatment That Could Protect Their Heart, Bones, and Brain.</title>
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			<title>Tavneos (Avacopan) and Serious Liver Injury: What Patients and Clinicians Need to Know — Including What the FDA Isn’t Saying Publicly</title>
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			<link><![CDATA[https://healthevidencedigest.com/fda-releases-draft-guidance-on-using-next-generation-sequencing-to-assess-safety-of-genome-editing-in-human-gene-therapy/]]></link>
			<title>The FDA Just Set New Rules for CRISPR Safety Testing. Here’s Why That Matters — and What It’s Actually Asking For.</title>
			<pubDate><![CDATA[Sat, 25 Apr 2026 14:08:03 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/fda-approves-higher-dose-semaglutide-under-national-priority-voucher-program/]]></guid>
			<link><![CDATA[https://healthevidencedigest.com/fda-approves-higher-dose-semaglutide-under-national-priority-voucher-program/]]></link>
			<title>Wegovy HD: The FDA Just Approved a Semaglutide Dose Three Times Stronger Than Before. Here’s What the Data Actually Shows.</title>
			<pubDate><![CDATA[Sat, 25 Apr 2026 13:16:55 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/fda-clears-aneuvos-exastim-system-for-spinal-cord-injury-therapy/]]></guid>
			<link><![CDATA[https://healthevidencedigest.com/fda-clears-aneuvos-exastim-system-for-spinal-cord-injury-therapy/]]></link>
			<title>Hands. Grip. Independence. What the FDA’s Clearance of the ExaStim® System Actually Means for Spinal Cord Injury Rehab.</title>
			<pubDate><![CDATA[Sat, 25 Apr 2026 12:14:04 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/fda-approves-gsks-lynavoy-for-cholestatic-pruritus-in-primary-biliary-cholangitis-pbc/]]></guid>
			<link><![CDATA[https://healthevidencedigest.com/fda-approves-gsks-lynavoy-for-cholestatic-pruritus-in-primary-biliary-cholangitis-pbc/]]></link>
			<title>That Itch That Won’t Quit: Inside the FDA Approval That PBC Patients Have Been Waiting For</title>
			<pubDate><![CDATA[Sat, 25 Apr 2026 11:45:08 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/fda-approves-first-generic-dapagliflozin-tablets/]]></guid>
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			<title>Generic Dapagliflozin Is Here. For 40 Million Americans With Type 2 Diabetes, That’s a Big Deal.</title>
			<pubDate><![CDATA[Sat, 25 Apr 2026 11:44:25 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/fda-approves-denali-therapeutics-avlayah-a-breakthrough-gene-therapy-for-hunter-syndrome/]]></guid>
			<link><![CDATA[https://healthevidencedigest.com/fda-approves-denali-therapeutics-avlayah-a-breakthrough-gene-therapy-for-hunter-syndrome/]]></link>
			<title>AVLAYAH Approved: For Hunter Syndrome Families, This FDA Decision Hits Different</title>
			<pubDate><![CDATA[Sat, 25 Apr 2026 00:44:18 +0000]]></pubDate>
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			<title>Welcome to Health Evidence Digest</title>
			<pubDate><![CDATA[Tue, 07 Apr 2026 11:39:42 +0000]]></pubDate>
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			<title>FDA Updates Its Review of GLP‑1 Medicines and Reports of Suicidal Thoughts</title>
			<pubDate><![CDATA[Sun, 05 Apr 2026 18:35:37 +0000]]></pubDate>
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			<link><![CDATA[https://healthevidencedigest.com/rocket-pharmaceuticals-secures-fda-approval-for-kresladi-a-landmark-gene-therapy-for-severe-lad-i/]]></link>
			<title>Rocket Pharmaceuticals Secures FDA Approval for KRESLADI™, a Landmark Gene Therapy for Severe LAD‑I</title>
			<pubDate><![CDATA[Sun, 05 Apr 2026 13:17:38 +0000]]></pubDate>
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			<pubDate><![CDATA[Sat, 25 Apr 2026 00:06:14 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/fda-requires-warning-about-vitamin-b6-deficiency-and-seizures-in-parkinsons-medications/]]></guid>
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			<title>FDA Requires Warning About Vitamin B6 Deficiency and Seizures in Parkinson’s Medications</title>
			<pubDate><![CDATA[Sat, 11 Apr 2026 01:54:00 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/teva-accelerates-its-biosimilar-strategy-with-new-fda-approval-and-dual-global-filings/]]></guid>
			<link><![CDATA[https://healthevidencedigest.com/teva-accelerates-its-biosimilar-strategy-with-new-fda-approval-and-dual-global-filings/]]></link>
			<title>Teva Accelerates Its Biosimilar Strategy With New FDA Approval and Dual Global Filings</title>
			<pubDate><![CDATA[Sat, 04 Apr 2026 22:22:59 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/fda-approves-foundayo-orforglipron-the-first-once-daily-glp-1-pill-for-weight-loss/]]></guid>
			<link><![CDATA[https://healthevidencedigest.com/fda-approves-foundayo-orforglipron-the-first-once-daily-glp-1-pill-for-weight-loss/]]></link>
			<title>FDA Approves Foundayo (Orforglipron), the First Once‑Daily GLP‑1 Pill for Weight Loss</title>
			<pubDate><![CDATA[Sat, 04 Apr 2026 22:04:24 +0000]]></pubDate>
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			<guid><![CDATA[https://healthevidencedigest.com/fda-approves-corcepts-lifyorli-for-platinum-resistant-ovarian-cancer/]]></guid>
			<link><![CDATA[https://healthevidencedigest.com/fda-approves-corcepts-lifyorli-for-platinum-resistant-ovarian-cancer/]]></link>
			<title>FDA Approves Corcept’s Lifyorli™ for Platinum‑Resistant Ovarian Cancer</title>
			<pubDate><![CDATA[Mon, 06 Apr 2026 01:43:00 +0000]]></pubDate>
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			<link><![CDATA[https://healthevidencedigest.com/fda-approves-first-once-weekly-basal-insulin-for-type-2-diabetes/]]></link>
			<title>FDA Approves First Once‑Weekly Basal Insulin for Type 2 Diabetes</title>
			<pubDate><![CDATA[Sat, 04 Apr 2026 19:11:03 +0000]]></pubDate>
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			<title>FDA Approves ICOTYDE™ (icotrokinra) for Moderate to Severe Plaque Psoriasis</title>
			<pubDate><![CDATA[Fri, 10 Apr 2026 01:30:00 +0000]]></pubDate>
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			<title>FDA Issues Complete Response Letter for Replimune’s RP1: What the Decision Means for This Oncolytic Immunotherapy</title>
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