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Evidence-based GLP-1 & peptide discussion since 2023
Forumsβ€ΊOral GLP-1 Agonistsβ€ΊHas anyone dealt with oral semaglutide bioavailability optimization?

Has anyone dealt with oral semaglutide bioavailability optimization?

quinn_sf Fri, Oct 25, 2024 at 3:30 PM 21 replies 1,668 viewsPage 1 of 5
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quinn_sf
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Oct 25, 2024 at 4:55 PM#1

Novo Nordisk's high-dose oral semaglutide 50mg program (OASIS trials) is attempting something ambitious: matching injectable semaglutide 2.4mg efficacy with an oral formulation. Let's break down the data.

The OASIS-1 trial (obesity without T2D) showed:[1]

  • 15.1% mean body-weight reduction at 68 weeks with oral sema 50mg
  • Compared to 2.4% with placebo
  • Approximately 85% of participants achieved ≥5% weight loss
  • Approximately 69% achieved ≥10% weight loss
  • Approximately 34% achieved ≥20% weight loss

For reference, injectable semaglutide 2.4mg in STEP-1 showed 14.9% mean weight loss at 68 weeks. So the oral 50mg dose is essentially matching the injectable in terms of efficacy.

The catch? It's still a peptide (not a small molecule like orforglipron), still requires the SNAC absorption enhancer, and still has the fasting/water administration restrictions. And the pill is physically large — 50mg of semaglutide + SNAC excipient makes for a sizable tablet.

[1] Knop FK, et al. Oral semaglutide 50 mg taken once daily in adults with overweight or obesity (OASIS 1). Lancet. 2023;402(10403):705-719.

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TirzTom
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Oct 25, 2024 at 5:12 PM#2

The fact that oral semaglutide 50mg matches the injectable at 2.4mg is a significant technical achievement, but I have mixed feelings about the practical implications.

The current Rybelsus (oral sema 14mg) already has significant adherence issues because of the administration requirements:

  1. Take on an empty stomach (no food for 2+ hours prior)
  2. Swallow with no more than 4 oz of plain water
  3. Wait at least 30 minutes before eating, drinking, or taking other meds

Those restrictions exist because SNAC only works in an empty stomach with minimal water to concentrate the local pH effect. The 50mg dose doesn't change any of that. You're still dealing with the same inconvenient administration.

Compare that to orforglipron: pop a pill, no restrictions. If I'm choosing an oral GLP-1, I know which one I'd prefer from a convenience standpoint.

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ChrisMacros
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Oct 25, 2024 at 5:29 PM#3

I've been on Rybelsus 14mg for the past 8 months and honestly... the restrictions aren't that bad once you build a routine. I take it first thing when I wake up, brush my teeth, shower, get dressed, and by then 30+ minutes have passed and I can have breakfast.

But I know I'm only getting a fraction of the efficacy compared to injectable. If the 50mg version truly matches Wegovy-level weight loss, I'd switch in a heartbeat. The convenience of no injections is worth the morning routine to me. πŸ’Š > πŸ’‰

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dave_SLC
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Oct 25, 2024 at 5:46 PM#4

Cross-trial comparison of oral vs. injectable semaglutide:

FormulationTrialMean WLDurationAdministration
Oral 14mgPIONEER 1~5%26 wksDaily, fasting
Oral 25mgOASIS-2~10%68 wksDaily, fasting
Oral 50mgOASIS-115.1%68 wksDaily, fasting
SC 2.4mgSTEP 114.9%68 wksWeekly injection

The dose-response curve is clear. And it demonstrates that oral semaglutide CAN match injectable — you just need a lot more drug to overcome the ~1% oral bioavailability. Hence 50mg oral = 2.4mg injectable (0.05 * 50mg ≈ 2.5mg absorbed).

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Dr.LeslieOBGYN
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Oct 25, 2024 at 6:03 PM#5

The manufacturing cost implication is important here. Even though oral sema 50mg matches the injectable in efficacy, you're using roughly 20x more semaglutide per dose compared to the injectable. That peptide isn't cheap to synthesize.

Rybelsus 14mg is already priced similarly to Ozempic. A 50mg version would require 3.5x more API per tablet. Whether Novo can price this competitively against the injectable while eating the higher COGS is an open question.

This is fundamentally the problem with oral peptides vs. oral small molecules. Orforglipron doesn't have this inefficiency because it's not a peptide — it doesn't need an absorption enhancer and has much higher oral bioavailability. The economics favor small molecules for oral delivery.

Last edited: Oct 26, 2024 at 12:03 AM
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