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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "Study Provides First In-D" (30 stories)

Top Headline Story

Accelerating and Modernizing Early and Late-Stage Clinical Development
Lead StoryU.S. Food and Drug Administration (.gov)general
Sep 21

Accelerating and Modernizing Early and Late-Stage Clinical Development

<a href="https://news.google.com/rss/articles/CBMiqwFBVV95cUxQUTVWQ2ZBOVFlRnBfeUwxRG5CRUU3ZU1vYk44NXE2TVUweHYyY2FsTkJuck5vdXJHa21RemQweEVibDJ3N2NSZkkxOVNuVVN0TUU5TTR0RjZyQkYwbnZSd3B4VTdmZHB5T0MtbEN5LWxhUlN4cVc2aVRKdHEtOVB6dVFxYTBPZHFCTGZxWUI4Z3ptSTdoYi12TkRRdzJ5SEd3RlpjV1J6SEJ2cGM?oc=5" target="_blank">Accelerating and Modernizing Early and Late-Stage Clinical Development</a>  <font color="#6f6f6f">U.S. Food and Drug Administration (.gov)</font>

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Search Results for "Study Provides First In-D"

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29 stories displayed
FDA's IND Pilot Puts CMC Review First
PharmTech.comgeneral

FDA's IND Pilot Puts CMC Review First

<a href="https://news.google.com/rss/articles/CBMid0FVX3lxTFBxZGE0QU9vQ2ViMlViM3NtZ2F2Mk9TNkRaUC1WRHBJcENaNEJvX0FfeWhCeGVOeDhSMEhXZzZ3XzY0SDdxTXdsNWFteFAwUTl5YVZXRzlFcDBvQ2M3Q3hQNXpmUWJPNG5ONWZXZ210dDNEN25wTW1n?oc=5" target="_blank">FDA's IND Pilot Puts CMC Review First</a>  <font color="#6f6f6f">PharmTech.com</font>

Insilico’s Rentosertib Inhalation Solution Receives IND Clearance for the World’s First AI-Driven Candidate to Enter Direct-to-Lung Clinical Study
Insilico Medicinetech

Insilico’s Rentosertib Inhalation Solution Receives IND Clearance for the World’s First AI-Driven Candidate to Enter Direct-to-Lung Clinical Study

<a href="https://news.google.com/rss/articles/CBMigwFBVV95cUxQaDk2MlEwRFQ2MklZYW11OWNPbXpwRkpvUURYTHF6WjRRQURnaE1laXRvTmd0SnNmUllaWWRXckVqZldvbjFzQkl5Sk14VXVFdDVBUVpPYmVxSGdhZ1ozbWtISzh4MFY2VWFwME1HamZSbUVXSXJPUUxYM1NNVmlKNk55MA?oc=5" target="_blank">Insilico’s Rentosertib Inhalation Solution Receives IND Clearance for the World’s First AI-Driven Candidate to Enter Direct-to-Lung Clinical Study</a>  <font color="#6f6f6f">Insilico Medicine</font>

Life Biosciences Announces FDA Clearance of IND Application for ER-100 in Optic Neuropathies
Life Biosciencesscience

Life Biosciences Announces FDA Clearance of IND Application for ER-100 in Optic Neuropathies

<a href="https://news.google.com/rss/articles/CBMiwwFBVV95cUxNdUlCamJkZURkcVgtZFlqZi0zWHNVSUFwcndSWWx3SkpVaEJEUXh2NU5PZm9falZlQS03SktoNUZRWXNDb1RYRFNrN3YyUHRPYXlfdEJ0R3Nud0JNX0Y0bk4tcHNrdlRqakhkVS14WjJ0enFSVGg0TGk2Sk9nN2kyeGpEOVJDWGNnYU8yV1NaSGdXSlBWcHdiRlBSVWxwel9PYVQyczk1bllPQmRab1h4WVpLWXBQZmthN19PV0h6bEx2N1U?oc=5" target="_blank">Life Biosciences Announces FDA Clearance of IND Application for ER-100 in Optic Neuropathies</a>  <font color="#6f6f6f">Life Biosciences</font>

FDA Clears Investigator-Initiated IND for SRN-101 in Recurrent High-Grade Glioma
CancerNetworkgeneral

FDA Clears Investigator-Initiated IND for SRN-101 in Recurrent High-Grade Glioma

<a href="https://news.google.com/rss/articles/CBMitgFBVV95cUxOblNiMXNzZzhVcUhnYmt5RHpGTG1YU0xmLTk0UEYwU1hiX21fQ3Y4clRpeHJfaXNDTWpaR0xqVVdjYWZaZkpwakY2U0xQNGNjY2U0WWhUc3NIaE5WeVdEeDNaU0doZXhZUnRrenQwRzgxaDIxeXpQR3FpYUFTSVU2eGJjNXltX0Z1YXFoMEFwbjkyV2VReGc1bUxTWEp5ZjlBOTFEdXNvZ3Vpc2JoYTJBZzVMZk1EQQ?oc=5" target="_blank">FDA Clears Investigator-Initiated IND for SRN-101 in Recurrent High-Grade Glioma</a>  <font color="#6f6f6f">CancerNetwork</font>

SMSbiotech Receives FDA "Study May Proceed" Notification for First U.S. IND-Cleared Inhaled Stem Cell Therapy in COPD
PR Newswiretech

SMSbiotech Receives FDA "Study May Proceed" Notification for First U.S. IND-Cleared Inhaled Stem Cell Therapy in COPD

<a href="https://news.google.com/rss/articles/CBMi_gFBVV95cUxNUDdXaWdMNUIwTEFveEk4T0NwRmc3Q2ZiNEhJajFCZWpDZUx6cnY4UmFqdDR4MElZRXFvYzh4aWduQkhoTVd4Wl9GYkFWdlJKUlR5a0ItaE5PMzNVa09yRmdjM09SSExXckNTeVpXcVlPai1zSk5zMmlRSlEyTVk2VjhUaTJ4STdmVFZ2bjJaYjlidjVrdXo2UU9sWl9FVUFzV1dVNjBOWG1SUEctcFNjUF9HWWNOcUZmTFAxY0d5NGZCM1QwbTJCbVZmQ0JDeG5vcjJBTUxFZVAwdTFNWTZkVFp0Si1OU3FFWEtQLWpreGJPb1lzQkhlRnptYVJlUQ?oc=5" target="_blank">SMSbiotech Receives FDA "Study May Proceed" Notification for First U.S. IND-Cleared Inhaled Stem Cell Therapy in COPD</a>  <font color="#6f6f6f">PR Newswire</font>

Humacyte Plans First Human Study of Bioengineered Vessel in Heart Bypass
Stock Titangeneral

Humacyte Plans First Human Study of Bioengineered Vessel in Heart Bypass

<a href="https://news.google.com/rss/articles/CBMiwAFBVV95cUxOdjNTZ2lxaUtvY1V4UjFSZ0hiSUpXcjE1WW5WVVpXVkZYTmkzNldldnZGZ21TajlLbGhuZThIU0JUbmVlMDZBQTRjcEdrZ1RvRnZqejMzcUxkU1U2cWpxSGt2eE5lY0x0bUNzOFM2ZGNXc0s2SE9Rei13MWJvOXVRYk9BNHBUUkZPc3djczFnZDNNdjZ4cWFIQkxPT09oMzgwdlV4MUZROGlad05KT2Voa2lWaEc2V3NzeWpuaEMtcTg?oc=5" target="_blank">Humacyte Plans First Human Study of Bioengineered Vessel in Heart Bypass</a>  <font color="#6f6f6f">Stock Titan</font>

Humacyte wins FDA IND clearance for first-in-human CTEV study in coronary artery bypass grafting
Dealroomgeneral

Humacyte wins FDA IND clearance for first-in-human CTEV study in coronary artery bypass grafting

<a href="https://news.google.com/rss/articles/CBMiygFBVV95cUxOeDRxdkNyZWhLc1p2YngySjBSMC1hY05fdlNOZ0pPN2JvZ0w0Um1DN0Y0MnZfWllsWHBfWG1aSFJLWEVBTGdBQTNXRllPZnJsaXlUU1ZlVXZXdXFsQ0o2UTR3M1BCb29qckFuVE1fTTFuNTF0SFFwcXNRcGxSNTAzaGhGdzB1d2FZUFM5NUJqWS1aR2E3QU5XVHVxNTBaRG5SWmJUa0RROXhxZ19yV1JfUUdRRkF3SWhqVXkwVklTVFQ5Z1EtLVlIeVBR?oc=5" target="_blank">Humacyte wins FDA IND clearance for first-in-human CTEV study in coronary artery bypass grafting</a>  <font color="#6f6f6f">Dealroom</font>

Ernexa Therapeutics Positioned to Become a Clinical-Stage Biotechnology Company as ERNA-101 On Track for Planned Q3 2026 IND Submission and First-in-Human Study
GlobeNewswiretech

Ernexa Therapeutics Positioned to Become a Clinical-Stage Biotechnology Company as ERNA-101 On Track for Planned Q3 2026 IND Submission and First-in-Human Study

<a href="https://news.google.com/rss/articles/CBMi0gJBVV95cUxNWGgtQ1FjTXFRakZhUGp2UXR1OWdYdWdDVkV4YWMxbXZieGg5Sm4ydmUwb3AzTzN1RnJ0aENKUk1QbGhVeHA4SVRtTkRQT3ZRRGZDMTg5SERGTk5oQzJkdS1CZWlkMGFOWURzdkYzVGlCUE5PRlAyY1M4ZTNKa3pON0p5SmNyQUJsQkE1Smp6YjRsdlowMW1reWxUVUxDVlJkTGtHUHZUZi1xeUF1MGNkcTZ0OHBLNDItNkh1Ymp0MmQwTVhPeDJRc09vM0dwUVdnSWl4TVN1dW5CRnA2V1BvaVhBWi1lVmk4MUk1dVJXUkd4aXVsY2pCaTFzbVBxN1N4YjRmSUxLTkFJQ3ZHemN0b2VRWDRlNHZ0b0hqTFRaUFpkN2Mya2Q4THBkMmxucXlscUNPMFR2NDVaeC1lb0V5ZFQ2WWl0MmF6RHV4RmpNX28xUQ?oc=5" target="_blank">Ernexa Therapeutics Positioned to Become a Clinical-Stage Biotechnology Company as ERNA-101 On Track for Planned Q3 2026 IND Submission and First-in-Human Study</a>  <font color="#6f6f6f">GlobeNewswire</font>

Arialys Therapeutics Announces First ANRE Patient Treated with ART5803 in Open-Label Phase 2 Study and FDA Clearance of IND for Randomized Phase 2 Study
Business Wireworld

Arialys Therapeutics Announces First ANRE Patient Treated with ART5803 in Open-Label Phase 2 Study and FDA Clearance of IND for Randomized Phase 2 Study

<a href="https://news.google.com/rss/articles/CBMiswJBVV95cUxPQmxEQjhWd3lUSXBteWszQkU2WE1ZQmc5UzVtUUlkZk5ZZ0o4YVMwZ1JhQlJmcjFnSGZvbnZxVXR6Y1BKRTV1M24zVlUzVG12WmFfUnlKeXBBd2R0VURiR19IYmJDbEExYVJlR0VySUxFWlVfNTg2QzJjMEpjczI0OWRJVEhTMTFQN3FXaS1VcmNJSFNWUUtob0FZMnBqMmpBOGtlSnRiZGdYa3lFVTJzLXRFVDN3LVo2MjdQZ25PZ29sVFJ2NVF5WG93OWVVTXliNTQ2OUJudXlvS1lPU2s1NHBibzdVaWRGcTh3RkpCb2RIa19uUkxrRlhWU2ZlTmJ5SS1idmZOdmU3MHdSR1VQdEFKcUd0VEJpb0xrRE1JVkpxQU9nbU5ERjcza1hFSGE5WTc4?oc=5" target="_blank">Arialys Therapeutics Announces First ANRE Patient Treated with ART5803 in Open-Label Phase 2 Study and FDA Clearance of IND for Randomized Phase 2 Study</a>  <font color="#6f6f6f">Business Wire</font>

Pheno Therapeutics gains FDA IND clearance for first-in-class GPR17 antagonist PTD802 in MS
Manufacturing Chemisttech

Pheno Therapeutics gains FDA IND clearance for first-in-class GPR17 antagonist PTD802 in MS

<a href="https://news.google.com/rss/articles/CBMijgFBVV95cUxQRjBwM3ZwQUozWUJzNUNNeW5hSkhYbHlrcWJxRTVEOTBjaWZPd3B1bmlybFBnalZCdVFYLXV2ZkxqODd3aTNsZTNIekdZTGpTclMzcWZiZ004dnBwMFNnbnc3Y2w2b0lZMU9SYTZtUkdfMTBOZW5jeVMtaHlKTXlKZ1JSYmFrelh6Ul9RZnZn?oc=5" target="_blank">Pheno Therapeutics gains FDA IND clearance for first-in-class GPR17 antagonist PTD802 in MS</a>  <font color="#6f6f6f">Manufacturing Chemist</font>

XtalPi Receives Second Payment from DoveTree; First Oncology Asset Advances into IND-Enabling Studies
PR Newswiregeneral

XtalPi Receives Second Payment from DoveTree; First Oncology Asset Advances into IND-Enabling Studies

<a href="https://news.google.com/rss/articles/CBMi7AFBVV95cUxPaVhsSDZMVmh6WDdPTG9hM0VuTkhaY1N0ZEZSUkZkUlhDUy1DSlBMUFAydmRTT3RRQkdlN1YyYWQwUDRUTThoZFVRTGRmMkdhRUFKQy1mRG8xRkVRQUV2X3hfVzlyWTg3Nk1MV2drUkMySnlhbDRsNGhjNFVYQmM0c3F2NF9GUjlseWdpNHBPQkRzVjFITzlEdXpzSVdtdnpaT0VCOGpyZXNla2dlYXJiQmFWNTY1a3pXbDk5cTRpcmFjUWRxaFFoVEU3VU5QbTRwTWJhLXBFZHVaRDUyWnZKOG5RLXZCWWlkbTdQOQ?oc=5" target="_blank">XtalPi Receives Second Payment from DoveTree; First Oncology Asset Advances into IND-Enabling Studies</a>  <font color="#6f6f6f">PR Newswire</font>

FDA Clears IND for Investigational Program in Recurrent High-Grade Glioma
CancerNetworkgeneral

FDA Clears IND for Investigational Program in Recurrent High-Grade Glioma

<a href="https://news.google.com/rss/articles/CBMirAFBVV95cUxPbXhYWDJGd2JUZndnVFVSSEhsVW9xN3E3TWl1T21qenNmdWd0WXNvTkNXdklZYnAyZ0ZiR3NXQ3JyUnF5R0NpVno4akJSQU1HOWZBRlRxTzZBZ0ppdlhCa3pjTFprcXlNYm5NM1FWSUV6eGFDcFJnelhWVEZDTEMxeVhobUhpWGdkbDV4UlRkU3ZzNmp6S1hXYjFna1hSYU55bFBoTjZJell1X2dQ?oc=5" target="_blank">FDA Clears IND for Investigational Program in Recurrent High-Grade Glioma</a>  <font color="#6f6f6f">CancerNetwork</font>

Calidi Biotherapeutics Receives Positive Pre-IND Feedback from US FDA for CLD-401 Indicating Agreement on its Current Development Strategy as it Advances Towards a First-in-Human Study
GlobeNewswiregeneral

Calidi Biotherapeutics Receives Positive Pre-IND Feedback from US FDA for CLD-401 Indicating Agreement on its Current Development Strategy as it Advances Towards a First-in-Human Study

<a href="https://news.google.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?oc=5" target="_blank">Calidi Biotherapeutics Receives Positive Pre-IND Feedback from US FDA for CLD-401 Indicating Agreement on its Current Development Strategy as it Advances Towards a First-in-Human Study</a>  <font color="#6f6f6f">GlobeNewswire</font>

DemeRx Announces FDA Acceptance of IND Application to Advance DMX-1001 for the Treatment of Alcohol Use Disorder (AUD)
Business Wireworld

DemeRx Announces FDA Acceptance of IND Application to Advance DMX-1001 for the Treatment of Alcohol Use Disorder (AUD)

<a href="https://news.google.com/rss/articles/CBMigwJBVV95cUxNX2NUTUhXdGdpZEhtWVlCbmNiR3dHbkhwVkZzeHloY01fWG5oOVBEbmlrZkNQSlY4NkhaZjRWZUZoTFRJRW5RNjVTTXNQSlo5TzhqVzBxT3NpR05EV0NnUm8ydl81X1VCT1FvcnNmbzBFUFdyYXVsMGNoTUNiUXF4VHlDU0RCX3kzNHpldDAwZ1A4Tm1RQVNQc0FEc0ZpYVlIeklrbzVaaV9FTU5JTGdfaHdFUG1qMDhVbVpXSjl5bWhxS21RN1hJMzQ4SlV2ZXpiY0ctQzVfalc0S2x2YjhOWmJJWU8zSVhxWlc5MEc3NFBkRlVaM0kzbURQcE81cjZoTU9N?oc=5" target="_blank">DemeRx Announces FDA Acceptance of IND Application to Advance DMX-1001 for the Treatment of Alcohol Use Disorder (AUD)</a>  <font color="#6f6f6f">Business Wire</font>

GH Research Reports First Quarter 2026 Financial Results and Provides Business Update
GlobeNewswiregeneral

GH Research Reports First Quarter 2026 Financial Results and Provides Business Update

<a href="https://news.google.com/rss/articles/CBMi7gFBVV95cUxPaGNDNzVySlNJTXJ4cUlGU0dUbGRwVW54OFZGWmhBZGllWEtEZkFCeW5jdEl1MW5KamJBSVNxRFF6Q1VCSl95THV6RFJoczdTeXlkVTBVemVGMjIxUU51Z0UySGtvTjNabVZfYnFxSXc3aEFrbmRnRDRxSGwxaW1vanZzcU1yZnZLazlDbXdwcVMzbU4wNjQydjVZcmR6dlNJNFQ5aFkxREtaUFA4YTBpUVZFanNPRkxLWDdYSXNUQy1SaVJiT3ViRnNvZ0JnNmRPc3JfR0xzVDlrUUFiX3B2SjBPc3h2emNQUmJhRS13?oc=5" target="_blank">GH Research Reports First Quarter 2026 Financial Results and Provides Business Update</a>  <font color="#6f6f6f">GlobeNewswire</font>

EndoCyclic Therapeutics Announces FDA Clearance of Investigational New Drug (IND) Application for ENDO-205, a First-in-Class Non-Hormonal Precision Peptide Therapeutic for Endometriosis
PR Newswireworld

EndoCyclic Therapeutics Announces FDA Clearance of Investigational New Drug (IND) Application for ENDO-205, a First-in-Class Non-Hormonal Precision Peptide Therapeutic for Endometriosis

<a href="https://news.google.com/rss/articles/CBMi2gJBVV95cUxPOW9oV0ZWZHo3OG1GVEliTWhvaXJzVGJCN0NMZFNvQWZRT0NraVBiZEhvcWo2dU4xTHpEek9DNkplR05zcEpDaF80MWRkUEd4OTVGMURSUEZjOHNmM0FNUFJobC0xZWxmR29JRzlpOE5rM0dYZE5JcFoyRmwzdW4xTjdrckpqSDZSVklxX2c5QlozbkhQbUZRZFJoRWhtTjUxNUFQQURIZmVmdFJ2aEZmN3IzME5JdWpjUXRKaUpZMDlBQlAzS1dHdHVSdHRidW9FOXR5VFVrX2kwV1lsc1h4eUcyZklFQXpGN183R2t2bndIeER1MWsyVF9BM0E2YjFDU21yc1FhSks2ZDM3N1RwMFd5elJHQUtmZHY4R21VYkFSVTc2X1MxN1hoUVNBWTdLQ01iTHd2QWpHeHJXcXh3dElLWHU0YnJMOGo0a0ViV0xEMnN4eUU1dHJ3?oc=5" target="_blank">EndoCyclic Therapeutics Announces FDA Clearance of Investigational New Drug (IND) Application for ENDO-205, a First-in-Class Non-Hormonal Precision Peptide Therapeutic for Endometriosis</a>  <font color="#6f6f6f">PR Newswire</font>

Foghorn Therapeutics Provides First Quarter 2026 Financial and Corporate Update
GlobeNewswiregeneral

Foghorn Therapeutics Provides First Quarter 2026 Financial and Corporate Update

<a href="https://news.google.com/rss/articles/CBMi4wFBVV95cUxQY1htWk8yR1BMcmxUOXdVQTV3U2ZBNTJpQnIwSjBZUGxFelVURWZYdEV2elU5ZnRtYUpjd0pSM1VqRjdEMmNqVHJhNmtYWjRpTk92OVZlU1RBRi1oaTBuQ1lLdXhGbUdjV082bGJUcjFiWGRKRGxscUZycE1wbWhhZTNlSkJEZGFpSHVJWmV5OVVlS2dPY3FlSmkzYl9LYThSTVZpSEwwbWM1bWZVNEV0VmR4NkNxUlR5dkIxWnJRTUp4MThrTU1hdlNJS1pSLTAxSlR3ZEQwNjUzMjhTXzJFeHZUZw?oc=5" target="_blank">Foghorn Therapeutics Provides First Quarter 2026 Financial and Corporate Update</a>  <font color="#6f6f6f">GlobeNewswire</font>

aTyr Pharma Announces First Quarter 2026 Results and Provides Corporate Update
GlobeNewswireworld

aTyr Pharma Announces First Quarter 2026 Results and Provides Corporate Update

<a href="https://news.google.com/rss/articles/CBMi5AFBVV95cUxQT1J1eFhLMlVhSUJDdkJKNGF4dTlLajVWd191VC1hdjcxYWVOSnNPbGJTNXo0MF9pRThOWGhKV200Q01xdEFwSjBHTngxcXJvNkd3Z29wdjJTa1NfSHFqSG5Ra1gyU1Mxd0RFbU04dk8xZDk0MWRON2JWOEVsNWJZMnVqYWJQZGZEYkhlVWREbnZwOGR6eUhPTmMwRFpyVk8xOG9zZ3N2NXF3SXZ1MDBULUtZMV9oYTJ5ODNHX2k3cUtGUjlIZm1VeTJsVUtWUDJiTGxMZmRkdmdfVEFnUWxKQU9mV0o?oc=5" target="_blank">aTyr Pharma Announces First Quarter 2026 Results and Provides Corporate Update</a>  <font color="#6f6f6f">GlobeNewswire</font>

Trace Biosciences Announces FDA IND Clearance for First Nerve-Specific Imaging Agent
BioSpacescience

Trace Biosciences Announces FDA IND Clearance for First Nerve-Specific Imaging Agent

<a href="https://news.google.com/rss/articles/CBMiwgFBVV95cUxNRk9MaVJhVHZyTzNOemRvaHNmR2Q3emFOYmM1LU5ROElQd2YxMVdwNGl5Y2tjTVRKUG44SWJMS1N3UE4ycDlnbE5hMUFrNHhCM1UxcTZsdWJSRUVGclI2bzBHYkZZRDlEampTWWZQZ2lBVVBXZzg2SGtYckU3ZVN4MnA3X1VXbWdaaU5YbHEzTHhSQndlSmVPUGlDeGNVelhjOGlfZVlqWmxuTWVTS3ZhaVRRR2Nvd0JiVF82SmxfNkR4Zw?oc=5" target="_blank">Trace Biosciences Announces FDA IND Clearance for First Nerve-Specific Imaging Agent</a>  <font color="#6f6f6f">BioSpace</font>

Pentixapharm Announces FDA Clearance of IND for Phase 3 PANDA Study of First-in-Class Cardiovascular Diagnostic Program
Lelezardworld

Pentixapharm Announces FDA Clearance of IND for Phase 3 PANDA Study of First-in-Class Cardiovascular Diagnostic Program

<a href="https://news.google.com/rss/articles/CBMizAFBVV95cUxNc3RHbXpnNkxQVU5KRWtLQ3A3Rko2UlZlR1U5d3hHc1p2ZDJhV1FsQnpFaEN1OVhMZjdIQVMxZHBVUXdXaWpsZk10RExKWVljamU1MFoySXVBazhSN21rbFF3LWlBVTAyanhUbXlUU1FZdVpvdTdpS3JqcS13SUVRcHd5aUk5U2ZZMEhQMUk5aWlkQmpuNnBMV3lwVVBEelVpU2NJU21DX2VqNVduVjF0clUwdUJPSTZfMUR0M1F6dkxMYW1xMnlqajV1bnI?oc=5" target="_blank">Pentixapharm Announces FDA Clearance of IND for Phase 3 PANDA Study of First-in-Class Cardiovascular Diagnostic Program</a>  <font color="#6f6f6f">Lelezard</font>

Enveda Announces US FDA IND Clearance and First Patient Dosed in Phase 1 Trial of ENV-308, a First-in-Class Oral Therapy for Obesity; Appoints Nadeem Sarwar, Ph.D., MPharm, MPhil, to Lead Metabolic Disease Strategy
BioSpaceworld

Enveda Announces US FDA IND Clearance and First Patient Dosed in Phase 1 Trial of ENV-308, a First-in-Class Oral Therapy for Obesity; Appoints Nadeem Sarwar, Ph.D., MPharm, MPhil, to Lead Metabolic Disease Strategy

<a href="https://news.google.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?oc=5" target="_blank">Enveda Announces US FDA IND Clearance and First Patient Dosed in Phase 1 Trial of ENV-308, a First-in-Class Oral Therapy for Obesity; Appoints Nadeem Sarwar, Ph.D., MPharm, MPhil, to Lead Metabolic Disease Strategy</a>  <font color="#6f6f6f">BioSpace</font>

VectorY Therapeutics Receives FDA Clearance of IND to Proceed with the PIONEER-ALS Phase 1/2 Trial of VTx-002, a First-in-Class Vectorized Antibody Targeting TDP-43 Pathology in ALS
Business Wiregeneral

VectorY Therapeutics Receives FDA Clearance of IND to Proceed with the PIONEER-ALS Phase 1/2 Trial of VTx-002, a First-in-Class Vectorized Antibody Targeting TDP-43 Pathology in ALS

<a href="https://news.google.com/rss/articles/CBMi1wJBVV95cUxNZzU3b3dSa1RxMHNrYUtZTHBHLVZnZy1fd29QTzJuVDVxZVphTGRDd09JYVpxaExYRjY4SEg5SFFVbjFSTUlLN216emFxSDVuVzc5U3ZIMjNiMkFtTGFmZzVtMUpfWV9hWDVQaHZqaUpzZG1rNTBmVU1SZmRjZTB4RnNRYUtPWjc2QmZXcm1WeGJNeWtZcDd3dWZ1N05jQzVWYnA1c1Q3VkRncXdSSC1SS3ItOEU3WjBFTkoxMnJLcXFxbExCY0lTR1Bwem05SUwwU3BUWDllWFBiSUpuVTN5QTZwbWVHTEIyYXMyLUNxZlpkeFJPRG02dUUxNi15SVpLUVNheW5od0lqbUJIRnRualVTclRmOTlMU3pjUWxsMThNbWZtQVlzcDkycjBlTUJfRExGdUZWeWJ0WnFBWS1kWDBOTmlYeDJZZzNQYzZyRmQ2V0JwUHMw?oc=5" target="_blank">VectorY Therapeutics Receives FDA Clearance of IND to Proceed with the PIONEER-ALS Phase 1/2 Trial of VTx-002, a First-in-Class Vectorized Antibody Targeting TDP-43 Pathology in ALS</a>  <font color="#6f6f6f">Business Wire</font>

First FDA IND Milestone Achieved Using Human Vascularized Organoid Efficacy Data
Fierce Biotechgeneral

First FDA IND Milestone Achieved Using Human Vascularized Organoid Efficacy Data

<a href="https://news.google.com/rss/articles/CBMivAFBVV95cUxNYU5keXB5YnJROWcxUlNMLXN2b1JIcTRyZzgwM0xyRThaNEFWN3M0UHIzOTQwZGVnWTNWLXFHSHR2NHRLOU51aWJxX1VDelBvb3IySzRMR0hMcFZmV01IUUREZ2tvS0I5SUxyQ0dPcU9jNWNGWURyX2xRUy1Pd0tiaC12bEtSRDBWQkZ2bFQ0cUo2ck9ISklZUGRMNzREb3BhYVlPWWVod21hRDF0QkVmcHNKY0M0Mkx0QWlBOQ?oc=5" target="_blank">First FDA IND Milestone Achieved Using Human Vascularized Organoid Efficacy Data</a>  <font color="#6f6f6f">Fierce Biotech</font>

Insilico Completes First-in-Human Dosing in Phase I Clinical Study of AI-Driven NLRP3 Inhibitor ISM8969, Achieving First Clinical Milestone in Collaboration with Hygtia Therapeutics
Insilico Medicinetech

Insilico Completes First-in-Human Dosing in Phase I Clinical Study of AI-Driven NLRP3 Inhibitor ISM8969, Achieving First Clinical Milestone in Collaboration with Hygtia Therapeutics

<a href="https://news.google.com/rss/articles/CBMigwFBVV95cUxNS2hZNDFtYnlhTGVjX242eld1UmNSQllWc3lON3RJampjRndaNHh5cDlMUUNxbTNiVERRdHNPcExNZER4amVDTmdvMEhnWFpIUGlTZXlTXzNIcDNIY3pxMjVRcmVJMGhtQVRGbVBtcl9sVUJyb3FVU1M0Qlg0WTJyOTdCUQ?oc=5" target="_blank">Insilico Completes First-in-Human Dosing in Phase I Clinical Study of AI-Driven NLRP3 Inhibitor ISM8969, Achieving First Clinical Milestone in Collaboration with Hygtia Therapeutics</a>  <font color="#6f6f6f">Insilico Medicine</font>

Cell Therapy Weekly: First IND Cleared for AAV-based Cancer Therapy
RegMedNetgeneral

Cell Therapy Weekly: First IND Cleared for AAV-based Cancer Therapy

<a href="https://news.google.com/rss/articles/CBMimAFBVV95cUxNWlRTclFoWmZBTllvdXR5dkhlWHVZVU4zeF9fam1mdlJreG9QOE1RY2FrbWl4VUZhTHQwUmxOUkU4UXJORnExdjQ3a3ZMUURjcmFPYkNVWFBtTWloZTZfck5ib1NVT05DNEdIQlJ0V1I0Q2hLNlNZQUpVU0lILW1HVFVQWTkyanpXaWdPUUF5Z1JLQmQxanJxdA?oc=5" target="_blank">Cell Therapy Weekly: First IND Cleared for AAV-based Cancer Therapy</a>  <font color="#6f6f6f">RegMedNet</font>

Press Release Service: Capsida Receives FDA IND Clearance for Its First-in-Class, IV-administered Gene Therapy for STXBP1 Developmental and Epileptic Encephalopathy
CRISPR Medicine Newspolitics

Press Release Service: Capsida Receives FDA IND Clearance for Its First-in-Class, IV-administered Gene Therapy for STXBP1 Developmental and Epileptic Encephalopathy

<a href="https://news.google.com/rss/articles/CBMi7wFBVV95cUxPajlhdkgzNkxUTVdOWWQ1ckZjSFZGTTBmaHFoaUF5WXF3UzFTRXlvRVJnUHE0VHZjTmtRLXBoel8tRDg4SkRCY3ltcmUweDcwSDV0MkhNLXVVRHFhUjVlRmlyWGk3M0xRbmkzVzRNTkIzZU1pZVVLS1lQOVZDRGVILTVLcS12cUw5enM0Ml9jb3QyYkpuMmhVa0tLR3lseElUZWNHdHJ5XzR1VEpDaVB3WHNlNUh4SmJJSmFoN2JxZ284WnMtNGZRUjJTUzQ2MHRZTnAwcXA3SURYVXRPd2JYQmRGME04ZmxobmR2Z2c5VQ?oc=5" target="_blank">Press Release Service: Capsida Receives FDA IND Clearance for Its First-in-Class, IV-administered Gene Therapy for STXBP1 Developmental and Epileptic Encephalopathy</a>  <font color="#6f6f6f">CRISPR Medicine News</font>

IDEAYA Biosciences Announces US FDA IND-Clearance for IDE849, a Potential First-in-Class DLL3 TOP1 ADC, for a Phase 1 Study in Solid Tumors
PR Newswirescience

IDEAYA Biosciences Announces US FDA IND-Clearance for IDE849, a Potential First-in-Class DLL3 TOP1 ADC, for a Phase 1 Study in Solid Tumors

<a href="https://news.google.com/rss/articles/CBMingJBVV95cUxPblB1emE4c05obmFMMEMyMWxTRHYtVHlKVi10UzdvblJRbks2WEVGRDFTUjhaaDFkOGNxM0lPRHpuT2I1bmhnZVJkOHYzNVFfaWxPMWk0VHZuVUZzQVZrNEp2bmplSEh5YnN1TF9SR2R2ZDdrdlhKTllQRUM4TDZUS0FxZHdTeVhJWVNXSXNVazFpaGMwLVBYSlE0aFNsUVBCbEhNVXd5a2dNcFF0c0FiOU5mMUNnNDF4N2M2bGRkYkFweFdXWnY2N3djMV9fd0EyMVBNVVFNa2JZSzJ2djd2UlNqWkFGVDhnVWtCN0JmUGhHT2M2RXYzN3VBTVJnZnZyWnZFS2xwTTlWN1VqWUdHZEFoOXJ3NnVaVXZ1TTRB?oc=5" target="_blank">IDEAYA Biosciences Announces US FDA IND-Clearance for IDE849, a Potential First-in-Class DLL3 TOP1 ADC, for a Phase 1 Study in Solid Tumors</a>  <font color="#6f6f6f">PR Newswire</font>

IDEAYA Biosciences Announces IND Clearance for IDE034, a Potential First-in-Class Bispecific B7H3/PTK7 TOP1 ADC Targeting Multiple Solid Tumor Types
PR Newswirescience

IDEAYA Biosciences Announces IND Clearance for IDE034, a Potential First-in-Class Bispecific B7H3/PTK7 TOP1 ADC Targeting Multiple Solid Tumor Types

<a href="https://news.google.com/rss/articles/CBMiqgJBVV95cUxPX3h0REhtUk1fYjV3WGtHbjVHbDdyQXg2U0pRRFVJdmpfZzhsS3lCUDR4TExHZ1RzMlJCWDNaTkVTU3hsa1NKdTRvYkpta3hhcHFDT013UVk2Q3IzN0Rheld5TmZEUXpBQTVUZVhIR044YzY5NENVUkZUcDhvTGRMWU90VmgxaUF6aU05R3FORU5BNWxvSnNRTmh6RU92aDRkYVFLdmRXdWVfZkplc01JWEFOZURFLWFkUjhSa09xWTJnR1pRbXh4R1h0ZzlRc2xpNXpQWWFvU05WQ0FVek9iSmRYV2FFZkxCODFRZTBmcnJmekxHQjlmY3FISVdYaVRBZVNkR1UxZzFUVXQyOVMtOGw2R1JBMzJPcy1fclRWMm9Gd2NuQ0YzLWp3?oc=5" target="_blank">IDEAYA Biosciences Announces IND Clearance for IDE034, a Potential First-in-Class Bispecific B7H3/PTK7 TOP1 ADC Targeting Multiple Solid Tumor Types</a>  <font color="#6f6f6f">PR Newswire</font>

First insight into metal binding proteins from the de novo transcriptome of acanthocephalan parasite Dentitruncus truttae
Natureworld

First insight into metal binding proteins from the de novo transcriptome of acanthocephalan parasite Dentitruncus truttae

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5yUWZPVkJHVFhCR2ItdXRKZjZIRjh0VmhrSGlQTWtudEpjN0xLakI5akVSalJBcWRMS1FZWlNZa0N0Y3FRbDFyemJVUm1vRUMtQXcxWGI1a0l6TUxjSzRr?oc=5" target="_blank">First insight into metal binding proteins from the de novo transcriptome of acanthocephalan parasite Dentitruncus truttae</a>  <font color="#6f6f6f">Nature</font>

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