When you hear the words Alzheimer's disease, what do you think of? The truth is, the picture most of us have of the disease is incomplete. Alzheimer's disease doesn't start when someone starts to lose their memory. It actually starts years – sometimes decades – earlier. The Rethinking Alzheimer's Disease Podcast is an engaging, narrative-style podcast miniseries for those curious or motivated to learn about Alzheimer’s disease. Perhaps you have a family member with Alzheimer’s disease, or ca ...
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HCPLive Podcasts에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 HCPLive Podcasts 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.
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HCPLive 5 Stories in Under 5: Week of 09/07
Manage episode 506489174 series 3310601
HCPLive Podcasts에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 HCPLive Podcasts 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.
Welcome to HCPLive's 5 Stories in Under 5—your quick, must-know recap of the top 5 healthcare stories from the past week, all in under 5 minutes. Stay informed, stay ahead, and let’s dive into the latest updates impacting clinicians and healthcare providers like you!
Interested in a more traditional, text rundown? Check out the HCPFive!
Top 5 Healthcare Headlines for September 5-September 14, 2025:
1. FDA Removes Sparsentan (Filspari) Advisory Committee Meeting for FSGS sNDA
The FDA determined no advisory committee is needed for sparsentan’s sNDA in FSGS, which remains under review with a January 2026 decision date.
2. Intercept Voluntarily Withdraws Obeticholic Acid (Ocaliva) for PBC From US Market
Intercept will withdraw obeticholic acid from the US PBC market after an FDA request and related clinical trial holds.
3. FDA Accepts FibroScan Letter of Intent for Surrogate Endpoint in MASH Trials
The FDA accepted a proposal to qualify FibroScan liver stiffness measurement as a surrogate endpoint for MASH trials, supported by multiple industry partners.
4. FDA Clears IND Application for EGEN-2784, a Genetically Engineered Pig Kidney, for ESKD
eGenesis received FDA clearance to begin clinical testing of a genetically engineered porcine kidney transplant in patients with ESKD.
5. First in Class Cat, Birch Allergen Blockers Succeed in Phase 3 Trials
Regeneron reported phase 3 success for novel allergen-blocking antibodies targeting cat and birch allergies, with confirmatory trials planned.
Interested in a more traditional, text rundown? Check out the HCPFive!
Top 5 Healthcare Headlines for September 5-September 14, 2025:
1. FDA Removes Sparsentan (Filspari) Advisory Committee Meeting for FSGS sNDA
The FDA determined no advisory committee is needed for sparsentan’s sNDA in FSGS, which remains under review with a January 2026 decision date.
2. Intercept Voluntarily Withdraws Obeticholic Acid (Ocaliva) for PBC From US Market
Intercept will withdraw obeticholic acid from the US PBC market after an FDA request and related clinical trial holds.
3. FDA Accepts FibroScan Letter of Intent for Surrogate Endpoint in MASH Trials
The FDA accepted a proposal to qualify FibroScan liver stiffness measurement as a surrogate endpoint for MASH trials, supported by multiple industry partners.
4. FDA Clears IND Application for EGEN-2784, a Genetically Engineered Pig Kidney, for ESKD
eGenesis received FDA clearance to begin clinical testing of a genetically engineered porcine kidney transplant in patients with ESKD.
5. First in Class Cat, Birch Allergen Blockers Succeed in Phase 3 Trials
Regeneron reported phase 3 success for novel allergen-blocking antibodies targeting cat and birch allergies, with confirmatory trials planned.
211 에피소드
Manage episode 506489174 series 3310601
HCPLive Podcasts에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 HCPLive Podcasts 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.
Welcome to HCPLive's 5 Stories in Under 5—your quick, must-know recap of the top 5 healthcare stories from the past week, all in under 5 minutes. Stay informed, stay ahead, and let’s dive into the latest updates impacting clinicians and healthcare providers like you!
Interested in a more traditional, text rundown? Check out the HCPFive!
Top 5 Healthcare Headlines for September 5-September 14, 2025:
1. FDA Removes Sparsentan (Filspari) Advisory Committee Meeting for FSGS sNDA
The FDA determined no advisory committee is needed for sparsentan’s sNDA in FSGS, which remains under review with a January 2026 decision date.
2. Intercept Voluntarily Withdraws Obeticholic Acid (Ocaliva) for PBC From US Market
Intercept will withdraw obeticholic acid from the US PBC market after an FDA request and related clinical trial holds.
3. FDA Accepts FibroScan Letter of Intent for Surrogate Endpoint in MASH Trials
The FDA accepted a proposal to qualify FibroScan liver stiffness measurement as a surrogate endpoint for MASH trials, supported by multiple industry partners.
4. FDA Clears IND Application for EGEN-2784, a Genetically Engineered Pig Kidney, for ESKD
eGenesis received FDA clearance to begin clinical testing of a genetically engineered porcine kidney transplant in patients with ESKD.
5. First in Class Cat, Birch Allergen Blockers Succeed in Phase 3 Trials
Regeneron reported phase 3 success for novel allergen-blocking antibodies targeting cat and birch allergies, with confirmatory trials planned.
Interested in a more traditional, text rundown? Check out the HCPFive!
Top 5 Healthcare Headlines for September 5-September 14, 2025:
1. FDA Removes Sparsentan (Filspari) Advisory Committee Meeting for FSGS sNDA
The FDA determined no advisory committee is needed for sparsentan’s sNDA in FSGS, which remains under review with a January 2026 decision date.
2. Intercept Voluntarily Withdraws Obeticholic Acid (Ocaliva) for PBC From US Market
Intercept will withdraw obeticholic acid from the US PBC market after an FDA request and related clinical trial holds.
3. FDA Accepts FibroScan Letter of Intent for Surrogate Endpoint in MASH Trials
The FDA accepted a proposal to qualify FibroScan liver stiffness measurement as a surrogate endpoint for MASH trials, supported by multiple industry partners.
4. FDA Clears IND Application for EGEN-2784, a Genetically Engineered Pig Kidney, for ESKD
eGenesis received FDA clearance to begin clinical testing of a genetically engineered porcine kidney transplant in patients with ESKD.
5. First in Class Cat, Birch Allergen Blockers Succeed in Phase 3 Trials
Regeneron reported phase 3 success for novel allergen-blocking antibodies targeting cat and birch allergies, with confirmatory trials planned.
211 에피소드
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