ArticlesSeptember 30, 2026·6 min read

ABBV-295: AbbVie Amylin Hits 9.8%, Eyes Monthly Dosing

AbbVie's amylin analog ABBV-295 reported up to 9.8% weight loss in 12 weeks, and a half-life that could support monthly dosing. What EASD 2026 showed.

A violet-glowing syringe on a dark surface in front of a faint circular arc of thirty light points

AbbVie presented the detailed Phase 1 data for ABBV-295, its long-acting amylin analog, at the EASD 2026 meeting in Milan on September 30. The study reported up to 9.8% mean weight loss at 12 weeks. The more notable result was the dosing interval: a mean half-life of 10.7 to 12.3 days, and a once-monthly cohort that still reported 7.9% weight loss at week 13.

Every amylin drug in late development today is dosed weekly. That includes cagrilintide, petrelintide and eloralintide. ABBV-295 is the first to put monthly-dosing data on a conference slide, and it comes from a company with no obesity drug on the market. AbbVie paid $350 million for the asset in 2025, and this is its first full dataset.

Research-context information only. Compounds discussed below are research peptides, investigational drugs, or approved pharmaceuticals depending on the molecule; several are not approved by the FDA. Protocols, doses, and outcomes reported come from published research and company disclosures. Possession or use of investigational drugs outside an authorized clinical trial may be illegal in your jurisdiction. This article reports what has been documented, not what should be done. Consult a licensed physician for personal medical decisions.

ABBV-295 has never been available outside AbbVie's clinical program, and no vendor lists it.

What AbbVie Presented at EASD

The numbers come from the multiple-ascending-dose portion (Parts 2B/2C) of a Phase 1 trial, NCT06144684, per AbbVie's September 30 release:

  • Design: randomized, double-blind within cohorts, placebo-controlled, single-center
  • Participants: 60 total (45 on ABBV-295, 15 on placebo); mean age 41.5, mean BMI 29.3, 88% male
  • Regimens: escalated to 4, 6 or 14 mg once weekly, 14 mg every other week, or 8 mg once monthly, for 12 to 13 weeks
Regimen Timepoint Reported mean weight change
Once weekly (4 / 6 / 14 mg cohorts) Week 12 -7.8% to -9.8%
Every other week (14 mg) Week 13 -9.7%
Once monthly (8 mg) Week 13 -7.9%
Placebo Week 12-13 about -0.3%

Pharmacokinetics. AbbVie reported a mean half-life of 10.7 to 12.3 days, a median time to peak concentration of 24 to 48 hours, and exposure that increased in proportion to dose. For comparison, a weekly-dosed peptide typically has a half-life of about a week. ABBV-295's half-life is closer to two weeks, which is what makes the every-other-week and monthly arms plausible.

Tolerability. Nausea was reported in 33.3% of ABBV-295 participants versus 20.0% on placebo, and diarrhea in 20.0% versus 0%. AbbVie reported 92% of gastrointestinal events as mild, no severe GI events, and a 4.4% discontinuation rate versus 0% on placebo. The March topline release said GI effects clustered in the first six weeks, which fits the escalation period.

"These detailed results showed meaningful weight loss alongside a half-life that could support dosing less frequently than once weekly," AbbVie's Dr. Primal Kaur said in the release. AbbVie moved ABBV-295 into Phase 2 in August 2026.

An abstract amylin receptor glowing violet with a long luminous peptide strand docking into it

How to Read a 12-Week, 60-Person Result

Three caveats limit how far these numbers can be pushed:

  1. It is 12 weeks. Amylin and GLP-1 weight loss curves are usually still falling at week 12. The number is an early slope, not an endpoint. Fierce Biotech reported William Blair's view that roughly 10% at week 12 is "competitive across the amylin class." That is a statement about trajectory, not about where the drug ends up.
  2. The cohort was 88% male with a mean BMI of 29.3. Obesity trials typically enroll majority-female populations with mean BMIs in the mid-to-high 30s. The same analysts suggested that more women in later trials could produce larger reported losses. Either way, the population is not comparable to other trials.
  3. Monthly is one cohort. The 7.9% monthly figure comes from a single small arm. Phase 2 is where AbbVie has to show that monthly dosing holds up against weekly dosing in a larger, more typical population.

What the data does establish is that the molecule works through the amylin receptor at a clinically meaningful level, and that its pharmacokinetics are unusual for the class.

What It Means for Buyers

Nothing in the research-compound market changes this week, for three reasons.

ABBV-295 cannot be sourced. It is a proprietary AbbVie molecule, and outside the trial it exists only in AbbVie's manufacturing chain. Listings claiming to sell it would be mislabeled.

Cagrilintide is the amylin analog research vendors actually list. Cagrilintide is Novo Nordisk's long-acting amylin analog and the amylin half of the semaglutide/cagrilintide combination. In the REDEFINE 1 Phase 3 trial, published in the New England Journal of Medicine, the combination reported 20.4% mean weight loss at 68 weeks versus 3.0% on placebo. Cagrilintide is also once-weekly, which puts the ABBV-295 half-life in context. The cagrilintide buying guide covers vendor COA practice and per-milligram pricing, and the cagrilintide price comparison lists live offers.

Amylin is now a pharma-validated mechanism. AbbVie, Roche, Lilly and Novo all have amylin programs in clinical development. Community sources describe pairing cagrilintide with GLP-1-class compounds, most often in the retatrutide/cagrilintide stack.

Vendor listings for cagrilintide and other research compounds are sold labeled for research use only. Current discount codes are collected on the peptide deals page.

Context: The Amylin Field After EASD 2026

ABBV-295 was one of several amylin presentations in Milan. The class now spans four large companies, and each is taking a different approach.

Four glowing glass vials in a row, each a different hue, suggesting competing amylin drug candidates

Compound Company Stage Reported headline result
Cagrilintide (with semaglutide) Novo Nordisk Under FDA review 20.4% at 68 weeks (REDEFINE 1, combination)
Eloralintide Eli Lilly Phase 3 20% at 48 weeks (Phase 2, amylin alone)
Petrelintide Zealand / Roche Phase 3 Up to 10.7% at 42 weeks (Phase 2)
ABBV-295 AbbVie Phase 2 Up to 9.8% at 12 weeks (Phase 1)

Zealand used the same meeting to present additional ZUPREME-1 data for petrelintide, published the same week in The Lancet Diabetes & Endocrinology. The paper reports up to 10.7% weight loss at 42 weeks (efficacy estimand) and GI rates comparable to placebo. Zealand said three Phase 3 trials are underway, plus a planned Phase 2 combining petrelintide with Roche's GLP-1/GIP agonist enicepatide. Our original ZUPREME-1 coverage covers the dose arms in detail.

Two strategies are emerging. Lilly's eloralintide and Zealand's petrelintide aim for amylin monotherapy that competes on tolerability. Novo's cagrilintide combination and its amycretin program aim to stack amylin on top of GLP-1. ABBV-295 adds a third variable, dosing frequency, which matters most for maintenance, where adherence falls off. Oral options such as the first oral amylin pill and Viking's VK3019 program are further behind.

None of the pipeline molecules exists as a lyophilized research powder. Research-vendor listings for cagrilintide, retatrutide and tirzepatide are lyophilized powders, and community documentation describes bacteriostatic water as the diluent used in reconstitution.

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Frequently Asked Questions

What is ABBV-295?
ABBV-295 is a long-acting amylin analog AbbVie acquired from Danish biotech Gubra in March 2025 (originally GUB014295) for $350 million upfront. It targets the amylin receptor rather than GLP-1, and its roughly 11-to-12-day half-life is designed to support dosing less often than once a week.
How much weight loss did ABBV-295 produce?
In the Phase 1 multiple-ascending-dose study presented at EASD 2026, AbbVie reported least-squares mean weight reductions of 7.8% to 9.8% at week 12 in the once-weekly cohorts, 9.7% at week 13 with every-other-week dosing, and 7.9% at week 13 with monthly dosing, versus about 0.3% on placebo. The study enrolled 60 participants, 88% of them male, with a mean BMI of 29.3.
Is ABBV-295 really a once-a-month drug?
The data support testing it that way. AbbVie reported a mean half-life of 10.7 to 12.3 days, and the 8 mg monthly cohort still reported 7.9% weight loss at week 13. That was a small, short Phase 1 cohort, though, and Phase 2 (started August 2026) is where dosing interval gets tested properly.
When could ABBV-295 be available?
Not soon. ABBV-295 entered Phase 2 in August 2026. A Phase 2 readout, a full Phase 3 program and FDA review typically take five or more years combined, which points to around 2031 at the earliest if every stage succeeds.
Is ABBV-295 sold by research peptide vendors?
No. ABBV-295 is a proprietary AbbVie molecule that exists only inside clinical trials. The amylin analog that research vendors do list is cagrilintide, the compound Novo Nordisk pairs with semaglutide. Live per-milligram cagrilintide pricing is compared on the /best/cagrilintide page.

References

  • AbbVie, "AbbVie Presents Detailed Phase 1 Data for ABBV-295, a Long-Acting Amylin Analog, Demonstrating Favorable Tolerability and Pharmacokinetic Profile at EASD 2026," September 30, 2026. prnewswire.com
  • AbbVie, "AbbVie Announces Positive Topline Results from a Phase 1 Multiple Ascending Dose Study of ABBV-295, a Long-Acting Amylin Analog, in Adults," March 9, 2026. news.abbvie.com
  • Fierce Biotech, "AbbVie ties $350M amylin bet to almost 10% weight loss after 12 weeks," March 2026. fiercebiotech.com
  • Garvey WT et al., "Coadministered Cagrilintide and Semaglutide in Adults with Overweight or Obesity" (REDEFINE 1), New England Journal of Medicine, 2025. PMID 40544433. nejm.org
  • Zealand Pharma, "Zealand Pharma to present additional data from Phase 2 ZUPREME-1 trial for petrelintide at EASD 2026 and announces publication of trial results in The Lancet Diabetes & Endocrinology," September 29, 2026. globenewswire.com