drug · protein
Wegovy
pre_registrationupdated 3mo agoby Novo Nordisk AS🔗 ChEMBL
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🐶 often sniffed alongside
top 8- drugOzempic222 co-mentions · 76 sources
- tagApproval176 co-mentions · 44 sources
- drugWegovy Pill168 co-mentions · 74 sources
- drugRybelsus121 co-mentions · 73 sources
- drugsemaglutide120 co-mentions · 72 sources
- tagSmall Molecule35 co-mentions · 18 sources
- tagRecall33 co-mentions · 27 sources
- companyNovo Nordisk Inc23 co-mentions · 4 sources
Protein drug with a maximum clinical stage of Approval (across all indications), with 6 approved and 30 investigational indications.
targets
Glucagon-like peptide 1 receptor
all catalysts(0)
nothing on the calendar yet
Trials studying Wegovy
- phase3A Research Study to See if Two Different Formulations of Oral Semaglutide Are Equally Safe and Effective in Reducing the Blood Sugar Level in Japanese People With Type 2 Diabetes
- phase1A Study to See the Effect of NNC0194-0499 Alone or in Combination With Semaglutide on Blood Sugar Control in People Living With Type 1 Diabetes
- phase3A Research Study to Compare Two Different Versions of Injectable Cagrilintide and Placebo in People With Excess Body Weight
- phase3A Study of BGM0504 in Early T2DM With Obesity
- phase2Obesity Complicating Type 1 Diabetes: GLP-1 Analogue Anti-obesity Treatment
- phase3A Research Study to Look at How Semaglutide Compared to Placebo Affects Diabetic Eye Disease in People With Type 2 Diabetes
- phase4Semaglutide Treatment, Appetite, and Eating Behavior: Long-term Effects
- phase1Semaglutide Delivered Epi-Intradermally by Microarray Patch (VX-201) Versus Subcutaneous Administration in Healthy Overweight and Obese Participants
News(10)
- STAT+: Pharmalittle: We’re reading about an FDA commish nominee, mRNA cancer vaccine results, and morePresident Trump is expected to nominate Heidi Overton, White House deputy director of domestic policy, to serve as the next FDA commissionerstat · 1d ago
- Enveda’s exercise-simulating obesity tablet clears early clinical testTouting an “exceptional” gastrointestinal safety profile for its oral obesity drug candidate in a study of healthy volunteers, Enveda plans to test the asset in people stopping GLP-1 treatment.biospace · 1d ago
- Novo takes first round of oral obesity duel. Can it stay ahead of Lilly?Despite coming away with an early victory over Eli Lilly in the oral obesity face-off, analysts don’t expect Novo Nordisk’s lead to last for very long.biospace · 1d ago
- Amylyx eyes FDA filing for GLP-1 blocker after late-stage win in post-bariatric hypoglycemiaWith a Phase 3 trial showing a reduction of serious and severe hypoglycemic episodes in patients who have undergone weight loss surgery, Amylyx Pharmaceuticals plans to file for approval this year.…biospace · 2d ago
- Amylyx readies approval push after GLP-1 inhibitor halves blood sugar crashes in ph. 3 winAmylyx Pharmaceuticals’ $35 million bet on the GLP-1 receptor antagonist avexitide appears to have paid off, with the molecule cutting the number of dangerous blood sugar crashes by more than half…fiercebiotech · 2d ago
- Skye and Redx form new entity with $125M to advance fibrosis assetsSkye Bioscience has entered into an agreement to combine with privately held fibrotic disease biotech Redx Pharma in a deal that will net $125 million in financing for the new public company, calle…fiercebiotech · 6d ago
- STAT+: Pharmalittle: We’re reading about California insulin sales, a Moderna patent battle, and moreSeven months after the launch of its own low-cost insulin brand, California has distributed more than 120,000 five-pen packs of insulin glargine priced at $55 eachstat · 7d ago
- Replimune finally wins approval, Q2 earnings wrap up, psychedelics stay in spotlightAfter two rejections, Replimune has made it across the regulatory finish line with its advanced melanoma therapy. Meanwhile, the last of the major pharmas, including Eli Lilly and Novo Nordisk, rep…biospace · 8d ago
- Scholar Rock rejigs approval filing after FDA flags violations at Novo plantDespite earlier claims of improvement at the fill-finish plant, the FDA has classified the facility as Official Action Indicated based on inspection findings.biospace · 9d ago
- After tasting IPO success, Hemab’s CEO seeks ‘flavor of a multi-product coagulation company’With the post-IPO quiet period having come to an end, CEO Benny Sørensen, M.D., Ph.D., was free to sit down with Fierce to map out Hemab’s future.fiercebiotech · 9d ago
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