Investigational — not approved or available to prescribe.
Main trial result
22%
Stage
Phase 2 → 3
Timeline (not confirmed)
2028+ (estimated — not confirmed)
Form
Weekly injection or daily pill
What it is
A single molecule that switches on both GLP-1 and amylin receptors. It hits the same two targets as CagriSema, but as one molecule rather than two drugs combined. A weekly injection and a daily pill are both in development. The early data shows exceptional promise: oral Phase 1 results came in ahead of oral semaglutide.
Why this matters:
Early oral data shows promise, but this is still Phase 1 and 2 data only. Larger Phase 3 trials will be the real test. These treatments are still under investigation, and results in larger trials may differ from early data.
Development stage and timeline
Current stage:
Phase 2 is complete for the injection, the oral form, and T2D. Phase 3 trials in obesity start in Q1 2026. Phase 3 in T2D is also planned.
Next milestone:
Phase 3 obesity trials enrolling 2026. Phase 3 T2D trials planned. Estimated approval: 2028+ (very preliminary; not confirmed).
How it works
One molecule designed to switch on GLP-1 receptors, which cut appetite and slow the stomach. It switches on amylin receptors too, which cut appetite and slow the stomach through brainstem pathways. Using a single molecule may make manufacturing simpler than a fixed-dose combination such as CagriSema.
Timeline note: The Phase 1 oral data showed significant weight loss within 12 weeks. The Phase 2 injection data covered 36 weeks
Early-stage data
Phase 1 and Phase 2 data only. Phase 3 trials are planned, but not yet complete. Treat these early results with caution.
In trial data, 22% mean weight loss vs. 2% weight gain in placebo (Phase 1b/2a)
In trial data, 13.1% weight loss vs. 1.1% placebo (Phase 1). Oral semaglutide reached about 6% at the same point.
In trial data, 14.5% weight loss in the Phase 2 T2D trial. 89.1% of patients reached HbA1c — a measure of average blood sugar over recent months — below 7%. Mean HbA1c drop of 1.8%.
Side effects (early-stage data)
Frequencies from Phase 2 trial data. Final Phase 3 safety profile may differ.
Notable findings
- ✓The pill showed 13.1% weight loss in 12 weeks — ahead of oral semaglutide at the same point (6%)
- ✓Single molecule may be simpler to manufacture than CagriSema's two-drug combination
- ✓Both injection and pill in development — offering a choice
What this tends to offer vs. what it involves
What this tends to offer
- ✓Promising early data: 22% (injection) and 13.1% (pill) in small trials
- ✓Single-molecule design simpler than two-drug combinations
- ✓Both injection and oral pill in parallel development
- ✓Oral formulation showing early signs of outperforming oral semaglutide
What this involves
- Very early stage — Phase 1 and 2 data only
- Phase 3 not starting until Q1 2026
- Approval likely 2028+ — years away
- No cardiovascular or long-term safety data yet
Community insights
These are personal experiences shared in public online communities — not medical advice.
“This is genuinely early — Phase 1 and small Phase 2 data only. The 22% and 13.1% numbers are exciting but from tiny, short studies.”
“The pill has no food timing restrictions, which comes up often as a key difference from oral semaglutide.”
Sources & references
- [1]Phase 1b/2a randomised controlled trial (subcutaneous)Adults with overweight or obesity · 36 weeks22% mean weight loss at 20 mg subcutaneous vs. ~2% weight gain in placebo. GI safety profile consistent with incretin class.Presented at EASD 2024 / Patient Care Online (2024) ↗
- [2]Phase 1 oral formulation trialAdults with overweight or obesity · 12 weeks13.1% weight loss at 2×50 mg/day vs. 1.1% placebo — exceeding oral semaglutide results at the same 12-week timepoint (~6%).EASD 2024 annual meeting / Patient Care Online (2024) ↗