Obesity drug catalyst calendar
Forward catalysts for the obesity drug race - earnings, trial readouts, and regulatory decisions - ordered by date and tiered by how much they move the stocks.
Forward calendar #
Catalysts ordered by date. Tier 1 events typically move the stock; Tier 2 are high-signal scientific or earnings reads; Tier 3 are mostly priced in.
| Date | Sponsor | Event | Tier | Category | Note |
|---|---|---|---|---|---|
| 2026 (ongoing) | Novo Nordisk | CagriSema HD Phase 3 initiated | 2 | trial start | Higher-dose CagriSema Ph3 program started Q2 2026 to test doses above 2.4/2.4 mg in obesity +/- T2D. |
| Jul 1, 2026 | Both | Medicare $50/mo cap takes effect | 1 | access | Trump administration deal: capped out-of-pocket cost of GLP-1s at $50/mo for eligible Medicare/Medicaid patients from Jul 1, 2026. Access tailwind - read post-July US volume against this, not as pure underlying demand. Applies to both Wegovy and Zepbound. |
| H2 2026 | Eli Lilly | Eloralintide + tirzepatide Phase 2 combo data | 2 | readout | Validates the amylin + incretin combo concept. Relevant to Zealand/Roche petrelintide + enicepatide combo and Novo zenagamtide unimolecular. |
| H2 2026 (est.) | Eli Lilly | Naperiglipron Phase 2 obesity readout (NCT06683508) | 2 | readout | First efficacy data on Lilly's second oral small-molecule GLP-1 (LY3549492). 36-wk weight endpoint, 5 doses + placebo, n=288. Trial COMPLETED per registry (primary completion Jan 2026); no disclosure date guided - timing estimated. Profile sets up the next-gen oral franchise behind Foundayo. |
| H2 2026 | Zealand Pharma | Petrelintide Phase 3 initiation | 1 | readout | Triggers $700M Roche milestone payment to Zealand. Confirms amylin platform momentum. |
| ~Mid-2026 | Roche | Enicepatide + petrelintide Phase 2 combo start | 2 | trial start | Roche to start the fixed-dose enicepatide (CT-388, GLP-1/GIP) + petrelintide (amylin) Phase 2 combination trial ~mid-2026. The combo is the differentiated bid for the high-weight-loss segment and the main reason petrelintides modest ~10.7% monotherapy is tolerated by the Street. 50/50 Roche/Zealand economics - also a key Zealand (.CO) catalyst. |
| Jul 31, 2026 | Both | 100% pharma import tariff effective (MFN exemption) | 1 | access | 100% ad valorem tariff on patented pharma imports takes effect Jul 31, 2026 for Annex III firms (Sep 29 for others); waived to 0% for companies signing MFN pricing + US onshoring deals. Novo (Denmark-manufactured GLP-1s) is the most exposed of the two; its Nov-2025 MFN deal secures the exemption, and Lilly is hedged by US onshoring. Watch for pricing/compliance read-through, not a demand signal. |
| Aug 5, 2026 | Novo Nordisk | Q2 2026 earnings | 1 | earnings | Same day as Lilly. First side-by-side commercial readout post-Wegovy pill launch. |
| Aug 5, 2026 | Eli Lilly | Q2 2026 earnings | 1 | earnings | Same day as Novo. First full quarter of Foundayo launch. Manufacturing CapEx + pricing commentary. |
| Aug 28 - Sep 1, 2026 | ESC | European Society of Cardiology Congress (Madrid) | 2 | conference | Possible ziltivekimab (NVO) CV data; cross-sponsor cardiovascular reads. |
| Sep 14-18, 2026 | EASD | EASD 2026 (Vienna, expected) | 2 | conference | CagriSema, zenagamtide, possibly eloralintide + tirzepatide combo Ph2 data. |
| Sep 20-21, 2026 | Novo Nordisk | Capital Markets Day | 1 | investor day | Major narrative-setting event under Doustdar. Peak-sales guidance, pipeline timelines. |
| ~Oct 2026 | Novo Nordisk | CagriSema FDA decision (PDUFA) | 1 | regulatory | NDA filed Dec 18, 2025; standard 10-mo review. First GLP-1+amylin combo approval; validates amylin platform. |
| Q4 2026 | Eli Lilly | Retatrutide FDA submission (Obesity + OA + OSA) | 1 | submission | First triple-indication GLP-1 submission. -28% to -30% weight loss. Sets up 2027 launch. |
| Q4 2026 | Eli Lilly | Foundayo OSA Phase 3 completion | 2 | readout | First non-T2D / non-obesity label expansion for orforglipron. |
| Q4 2026 | Novo Nordisk | Q3 2026 earnings | 2 | earnings | Will include CagriSema PDUFA outcome if decided by then. |
| Q4 2026 | Boehringer Ingelheim | Survodutide regulatory submission (obesity) | 1 | submission | Per Steensberg (Zealand): 'later this year.' Positions BI as the third obesity-injectable player after Novo + Lilly. Launch expected 2027. |
| ~Oct 29, 2026 | Eli Lilly | Q3 2026 earnings | 2 | earnings | Foundayo full launch quarter; Retatrutide submission update. |
| Nov 7-10, 2026 | AHA | AHA Scientific Sessions | 2 | conference | More CV data; possible retatrutide CV biomarkers; ziltivekimab follow-on. |
| 2027 | Boehringer Ingelheim | Survodutide obesity launch | 2 | launch | Third obesity injectable on the market after Wegovy/Zepbound. |
| 2027 | Eli Lilly | Retatrutide vs tirzepatide head-to-head trial begins | 3 | readout | First internal Lilly head-to-head between retatrutide and tirzepatide. Readout 2028+. |
| 2027 | Novo Nordisk | Cagrilintide monotherapy Phase 3 readout | 2 | readout | Cagrilintide as standalone obesity drug (non-incretin amylin analog), separate from CagriSema combo. |
| Early Jan 2027 | JPM | J.P. Morgan Healthcare Conference | 2 | conference | Annual sell-side presentation; all major obesity players give pipeline guidance. |
| Q1 2027 | Eli Lilly | Retatrutide T2D FDA submission | 2 | submission | T2D label expansion for triple agonist after obesity/OA/OSA submission. |
| H1 2027 | Novo Nordisk | REDEFINE-11 CagriSema Ph3b readout | 2 | readout | Phase 3b cohort, additional CagriSema data per Novo R&D Day 2026. |
| H1 2027 | Novo Nordisk | UBT251 global Ph1b/2a obesity readout | 2 | readout | Global expansion of UBT251 (GLP-1/GIP/glucagon triple agonist licensed from United Biotech). Ph2 China at 6mg/24wk showed -19.7%. |
| Early Feb 2027 | Novo Nordisk | FY 2026 earnings + guidance | 2 | earnings | Annual reset; full-year guidance for 2027 incl. CagriSema launch trajectory if approved. |
| H2 2027 | Novo Nordisk | REDEFINE-3 CagriSema CVOT readout | 1 | cv outcomes | Cardiovascular outcomes trial - thesis-defining for CagriSema commercial trajectory; CV-event reduction would unlock label expansion + payer coverage. Per Novo R&D Day 2026. |
| 2028+ | Eli Lilly | ENLIGHTEN Phase 3 readouts (Eloralintide) | 3 | readout | 5 trials (ENLIGHTEN-1 through -4 and -6). Amylin platform validation. |
| 2028+ | Novo Nordisk | AMAZE Phase 3 readouts (Zenagamtide) | 3 | readout | 7 trials (AMAZE 1-6 and 12), 84-week duration. Unimolecular GLP-1+amylin validation. |
No catalysts match the selected filters.