Scientific deep-dive

The Next GLP-1 Pills: Elecoglipron, Aleniglipron and Other Oral Drugs in Trials

A wave of daily small-molecule GLP-1 pills is moving through trials after Foundayo and the Wegovy pill. What 2026 trials of elecoglipron, aleniglipron, HRS-7535, VCT220, safiglipron and TERN-601 showed, why TERN-601 was dropped, and why none is available yet.

By Eli Marsden · Founding Editor
Editorially reviewed & fact-checked against primary sources · How we verify contentLast reviewed
8 min read·9 citations

Two GLP-1 pills for weight loss are already approved in the US: Foundayo (orforglipron) and the Wegovy pill (oral semaglutide). Behind them is a wave of new daily tablets, most of them small molecules like orforglipron rather than peptides like semaglutide. In 2026 the first big trials of several were published: elecoglipron (up to −10.5% at 26 weeks), aleniglipron (up to −11.3% placebo-adjusted at 36 weeks), and Chinese candidates HRS-7535, VCT220 and safiglipron.[1][3][4][5][6][7] Another, TERN-601, was discontinued after liver-safety findings.[8] Here is what each trial showed and why none will reach pharmacies soon.

About this article

Everything here is investigational unless stated otherwise. Results come from peer-reviewed phase 1–3 trials, most sponsored by the drug developers. Trials differ in length, dose and population, so their numbers can't be compared directly. For the pills you can get today, see our comparison of approved GLP-1 pills. This is not medical advice.

The short answer

  • Small-molecule pills are the trend. Unlike oral semaglutide, these are non-peptide drugs, and at least one, safiglipron, is taken without fasting or food restrictions.[5]
  • Phase 2 weight loss so far is in the 7–11% range over 16–36 weeks at the higher doses.[1][3][4][7]
  • Side effects match the injectable GLP-1s: mainly nausea, vomiting, diarrhea and constipation, most common during dose escalation.[4][7]
  • Liver safety is the thing to watch. TERN-601's phase 2 study reported three cases of liver-enzyme elevations consistent with possible drug-induced liver injury, and its developer then stopped clinical development.[8]

The candidates

Oral small-molecule GLP-1 drugs with published 2026 trial results
DrugTrialWhoResultNotes
ElecoglipronVISTA, phase 2, Lancet310 adults with obesity/overweight−2.6% to −10.5% at 26 wk (placebo −0.6%)Up to 88.8% reached ≥5% loss
ElecoglipronSOLSTICE, phase 2b, Lancet404 adults with type 2 diabetesHbA1c −0.91% to −1.88% at 26 wkGI events most common
AleniglipronACCESS, phase 2b, Nat Med230 adults with obesity/overweightPlacebo-adjusted −8.2% to −11.3% at 36 wk“No apparent weight-loss plateau”
HRS-7535Phase 2, Nat Commun235 Chinese adults with obesity, no diabetesPlacebo-adjusted up to −6.87% at 26 wk60 mg and above effective
VCT220Phase 2, China250 adults with overweight/obesity−5.75% to −9.73% at 16 wk (placebo −1.61%)Lifestyle counseling included
SafiglipronOUTSTAND-1 and -2, phase 3, Nat MedAdults with type 2 diabetes in ChinaHbA1c down up to −1.45% vs placeboTaken without fasting or food restrictions
TERN-601Phase 1 and 2, ObesityAdults with obesity/overweightGreater weight loss at ≥500 mg by week 123 possible drug-induced liver injury cases; development discontinued

Elecoglipron

Two phase 2 trials appeared in The Lancet in 2026. In VISTA, 310 adults with obesity or overweight (mean BMI 38.2) lost between 2.6% (5 mg) and 10.5% (75 mg with weekly titration steps) at 26 weeks, against 0.6% on placebo, and 40.4–88.8% reached at least 5% weight loss, against 15.6%. Adverse events were reported by 84–98% on elecoglipron and 84% on placebo, mostly nausea, constipation, diarrhea, headache and vomiting.[1] In SOLSTICE, in type 2 diabetes, HbA1c fell between 0.91% and 1.88% at 26 weeks, against 0.15% on placebo.[2]

Aleniglipron

The ACCESS phase 2b trial randomized 230 adults (mean BMI 39.5) to daily aleniglipron escalated every 4 weeks to 45, 90 or 120 mg. At 36 weeks, placebo-adjusted weight change was −8.2%, −9.8% and −11.3%, “with no apparent weight-loss plateau.” Treatment-related discontinuations were 10.4%, “with no events of drug-induced liver injury.”[3]

HRS-7535, VCT220 and safiglipron (China)

HRS-7535 produced placebo-adjusted weight loss of 4.60% at 60 mg and 6.87% at 180 mg over 26 weeks; the 30 mg dose did not beat placebo.[4] VCT220 reduced weight by 5.75% (80 mg) to 9.73% (160 mg) at 16 weeks, against 1.61% on placebo.[7] Safiglipron, which “is administered without fasting or dietary restrictions,” has reached phase 3 in type 2 diabetes. It lowered HbA1c by up to 1.45 points against placebo and was non-inferior to dapagliflozin, though its weight loss was modest: up to 3.56% against placebo.[5][6]

TERN-601: discontinued over liver safety

TERN-601 produced dose-dependent weight loss in phase 1 and significantly more weight loss than placebo at 12 weeks on doses of 500 mg or more in phase 2. But “three participants in the Phase 2 study experienced transaminase elevations consistent with potential drug-induced liver injury.” Those findings “led to clinical development discontinuation.”[8] Liver safety is watched closely for this class; the aleniglipron trial, for example, reported explicitly that there were no drug-induced liver injury events.[3]

Why small-molecule pills matter

  • Easier to take. The Wegovy pill must be taken “on an empty stomach in the morning with water (up to 4 ounces),” followed by a 30-minute wait before eating or drinking.[9] Some small molecules, including safiglipron, are taken without fasting or food restrictions.[5] See how to take Foundayo for the approved example.
  • No injections or cold storage. A tablet avoids pens and refrigeration.

When could they be available?

Not soon. Elecoglipron and aleniglipron have published phase 2 results but still need phase 3 trials before their developers can apply for FDA approval. HRS-7535, VCT220 and safiglipron have so far been tested only in China. None of these pills can be legally prescribed or compounded in the US. Products sold online under these names are not the real drugs. In the meantime, see the Foundayo approval and the Wegovy pill guide.

Bottom line

A new generation of daily GLP-1 pills is moving through trials, with phase 2 weight loss of about 7–11% over 16–36 weeks and the familiar GI side effects. The most advanced in obesity are elecoglipron and aleniglipron. Liver safety is the key open question for the class. For people who want a pill today, Foundayo and the Wegovy pill are the approved options.

Frequently Asked Questions

Oral small-molecule GLP-1 drugs with 2026 trial results include elecoglipron, aleniglipron, HRS-7535, VCT220 and safiglipron. A sixth, TERN-601, was discontinued after liver-safety findings. None is FDA-approved. The approved GLP-1 pills for weight loss in the US are Foundayo (orforglipron) and the Wegovy pill (oral semaglutide).
In phase 2 trials, aleniglipron produced placebo-adjusted weight loss of up to 11.3 percent at 36 weeks, elecoglipron up to 10.5 percent at 26 weeks, VCT220 up to 9.7 percent at 16 weeks, and HRS-7535 up to 6.9 percent placebo-adjusted at 26 weeks. Trials differ in length and design, so the numbers are not directly comparable.
It depends on the drug and is still being studied. TERN-601's phase 2 study reported three cases of liver-enzyme elevations consistent with possible drug-induced liver injury, and its development was discontinued, while the aleniglipron phase 2b trial reported no drug-induced liver injury. Liver safety is a key question for this drug class.
Not soon. Both have published phase 2 results but still need phase 3 trials before their developers can apply for FDA approval. They cannot be legally prescribed or compounded in the US today.

References

  1. 1.Davies MJ, Aroda VR, Rosenstock J, Capehorn M, Pedersen SD, Morizzo E, et al. Elecoglipron, an oral small molecule GLP-1 receptor agonist in adults with obesity or overweight (VISTA): a multicentre, phase 2, randomised, placebo-controlled clinical trial Lancet. 2026;407(10547):2503-2514. 2026. PMID: 42259337.
  2. 2.Aroda VR, Davies MJ, Maaske J, Millegård M, Juan VL, Aberle J, et al. Elecoglipron, an oral small molecule GLP-1 receptor agonist in adults with type 2 diabetes (SOLSTICE): a multicentre, phase 2b, randomised, placebo-controlled trial Lancet. 2026;407(10547):2515-2527. 2026. PMID: 42259343.
  3. 3.Rosenstock J, Lingvay I, Ryan D, Jastreboff AM, Kushner R, Acosta A, et al. Oral small molecule GLP-1 receptor agonist aleniglipron in people with overweight or obesity: a randomized, double-blind, placebo-controlled phase 2b trial Nat Med. 2026;32(8):2941-2947. 2026. PMID: 42249138.
  4. 4.Gu W, Zhang L, Li L, Wei D, Li Q, Zong Y, et al. HRS-7535, an oral small-molecule GLP-1 receptor agonist, in Chinese adults with obesity without diabetes: a randomized, double-blind, placebo-controlled phase 2 trial Nat Commun. 2026;17(1):7867. 2026. PMID: 42331800.
  5. 5.Yu M, Peng L, Jiang C, Zhang X, Li Q, Zhang L, et al. Oral small-molecule GLP-1 receptor agonist safiglipron in early type 2 diabetes: a randomized, double-blind, placebo-controlled trial Nat Med. 2026. 2026. PMID: 42811187.
  6. 6.Guo L, Yu D, Xu Y, Tang G, Peng L, Meng C, et al. Oral small-molecule GLP-1RA safiglipron versus dapagliflozin in type 2 diabetes: a randomized, double-blind, active-comparator-controlled phase 3 trial Nat Med. 2026. 2026. PMID: 42834229.
  7. 7.Ji L, Gao L, Li B, Liu M, Zhang X, Meng C Oral nonpeptide GLP-1 receptor agonist VCT220 for obesity treatment: a randomized, double-blind, phase II trial Signal Transduct Target Ther. 2026;11(1):325. 2026. PMID: 42595749.
  8. 8.Garvey WT, Rosenstock J, Bays HE, Denham D, Kohli A, Haines M, et al. Oral GLP-1RA TERN-601 for Adults With Obesity/Overweight: Placebo-Controlled, Multiple-Ascending-Dose, Phase 1 and 2 Studies Obesity (Silver Spring). 2026;34(9):1742-1758. 2026. PMID: 42528333.
  9. 9.Novo Nordisk WEGOVY (semaglutide) injection and tablets — US Prescribing Information (Section 2.1) DailyMed, SetID ee06186f-2aa3-4990-a760-757579d8f77b. 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ee06186f-2aa3-4990-a760-757579d8f77b

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