STUDresearch · Peptide
Ribupatide
Also known as
HRS-9531 · HRS9531 · KAI-9531 · Kailera / Hengrui dual GLP-1/GIP · ribupatide oral · ribupatide injection
Community talk. May be wrong. Not medical advice. Not a protocol. Not for human or animal use.
Systemic dual GLP-1/GIP — weekly injection (KaiNETIC / China Phase 3) and a separate once-daily oral program.
Weight loss and little nausea were reported, but unknown allocation means exposure was unconfirmed.
567-participant, 48-week trial; 6 mg treatment-policy mean loss was 17.7% versus 1.4% placebo.
Separate 36-week trial; company reported 23.6% mean loss from baseline versus 1.8% placebo.
166-adult China trial over 26 weeks; oral tablet amounts are not injectable equivalents.
Planned Phase III exposure through 76 weeks; no outcome follows from the maximum.
Half-life & effect duration
- Half-life in the body
- Injected · company study estimateAbout 1 week
- Felt duration people report
- Blinded trial accountLittle nausea around month 4; occasional nausea or heartburn later
- Within-week durationNot consistently reported
Tap a line to jump into the full notes. Research only — may be wrong.
Timing context & sources
Half-life in the body
A company-reported Phase Ib injection study estimated ribupatide terminal half-life at about one week.
Adults with type 2 diabetes received weekly SC HRS9531 across 0.3–4.5 mg for four weeks; the report says terminal half-life about one week and single-dose median Tmax 72.0–94.8 hours.
Conference/company summary, approximate value, short exposure, diabetes population and injectable formulation; not transferable to oral tablets.
- Hengrui — HRS9531 injection Phase Ib in type 2 diabetes (opens in a new tab)63 participants received at least one treatment; 0.3/1.5/up-to-4.5 mg SC weekly for four weeks. Company conference report says terminal half-life about one week and single-dose median Tmax 72.0–94.8 h.Chinese-language company conference summary, not a full peer-reviewed PK table; approximate and formulation-specific.
Felt duration people report
No ribupatide-specific per-dose felt-duration window was established in the inspected community evidence.
A blinded participant described little nausea around four months and occasional nausea/heartburn later, but unknown assignment means exposure was unconfirmed and no within-week clock was reported.
One anonymous blinded account without verified assignment, records or per-dose timing; class expectations cannot substitute.
- Reddit r/Zepbound — Starting journey in a ribupatide trial (opens in a new tab)Same author reported blinded study participation, 3 mg weekly around four months, 23 lb loss/little nausea, then 37 lb since April with occasional nausea/heartburn.Blinded assignment: author could not know ribupatide versus comparator/placebo; anonymous, no records, no per-dose clock.
Other context in this card
- Kailera — Additional Phase III HRS9531 obesity data (opens in a new tab)NCT06396429: 567 Chinese adults, weekly SC 2/4/6 mg or placebo for 48 weeks; treatment-policy mean loss 17.7% at 6 mg versus 1.4% placebo; hypothetical estimand 19.2%.Company-sponsored release linked to registered/conference work; estimands must stay separate and generalization is limited.
- Kailera — Phase II obesity topline for oral ribupatide (opens in a new tab)166 adults in China: oral 10/25/50 mg daily for 26 weeks produced efficacy-estimand losses 6.9/12.1/12.1%; separately cites 23.6% at week 36 for 8 mg injectable Phase II.Company topline; oral/injectable forms, dose scales and phases are not interchangeable.
- Kailera — First participants randomized in KaiNETIC Phase III (opens in a new tab)Three global double-blind randomized Phase III trials evaluate weekly SC doses up to 10 mg over 76 weeks.Program description, not an outcome or recommended regimen.
- Kailera — Second-quarter 2026 ribupatide high-dose trial update (opens in a new tab)The fully enrolled U.S. Phase IIb trial NCT07458269 includes 264 adults with BMI at least 35 and no type 2 diabetes, evaluating 10, 13, 16 or 20 mg injection once weekly over 48 weeks.Company trial-status report, not an outcome; maximum planned exposure does not establish efficacy, tolerability or a recommended regimen.
What people say
- Class dual appetite: Import tirz food-noise talk until there is a real English logbook. forum
- China injection trials: Phase II reported 23.6% mean loss from baseline at 8 mg by week 36 versus 1.8% placebo. Separate Phase III reported 17.7% at 6 mg by week 48 versus 1.4% placebo under the treatment-policy estimand; the hypothetical estimand was 19.2%. trial
- Oral Phase 2: Up to ~12.1% at 26 weeks, no plateau in the press line. trial
- KaiNETIC: Three global Phase 3 weekly-injection trials, data talked as 2028. trial
Doses people talk about
- Do not put 25 mg oral on a 10 mg pen. forum
- US high-dose 2b: Weekly up to 20 mg, 48 weeks, BMI≥35, readout talked 2027. trial
- China injectable quotes: 6 mg and 8 mg weekly in the % headlines. trial
- Injectable Phase 3 (KaiNETIC talk): Weekly SC up to 10 mg over ~76 weeks. trial
- Oral Phase II: 10, 25 or 50 mg once daily for 26 weeks; company topline reported 6.9%, 12.1% and 12.1% mean loss from baseline under the efficacy estimand. Oral and injectable milligrams are not interchangeable. trial
How it may feel
- Blinded participant account: A U.S. trial participant reported reaching 3 mg weekly around four months, losing 23 lb with little nausea, and later 37 lb since April with occasional nausea and heartburn. Allocation was blinded, so this cannot identify ribupatide as the cause. anecdote
- Oral vs pin: Two feel curves. Oral 26-week 12% will not feel like an 8 mg China pin. forum
- If a Discord vial says HRS-9531: Assume identity risk first, feel-curve second. forum
Cycles people discuss
- Weekly injection, chronic. trial
- Oral daily, chronic, China-first. trial
Timing
- Injectable designed weekly — long-acting dual peptide. Public English t½ tables are thinner than tirz; do not invent hours. forum
- Oral is a different PK problem. trial
More on what it is
- Feel-log honesty: US diary layer is thin. Most “how it feels” is class dual + China-trial tables. forum
- What it is: Hengrui’s dual agonist. Injectable = HRS-9531 / KAI-9531 (Kailera’s global name ribupatide). There is also an oral ribupatide. Not tirz. Not approved in the US. trial
- Why people talk about it: Separate China injection trials reported 23.6% mean loss from baseline at 8 mg by week 36 in Phase II and 17.7% at 6 mg by week 48 in Phase III under the treatment-policy estimand. These are company-reported trial results, not one combined Phase III figure. trial
- How it works: Dual incretin — same cartoon as Mounjaro. trial
- Two products: Weekly pin (global Phase 3 up to 10 mg, high-dose 2b up to 20 mg) vs daily oral (China Phase 3 bound; ~12% at 26 weeks in an oral Phase 2). Do not mash the mg. trial
Stacks
- Mental stack: vs tirz / enicepatide / mazdutide. forum
- Solo in the trials. trial
Storage notes
- No STUD mix chart. “HRS-9531” research vials are not KaiNETIC drug. forum
Watch for
- Geography: China % may not copy onto a US body — that is the KaiNETIC question. forum
- Two modalities, two mg languages. forum
- Unapproved in the US. forum
- Gray dual vials. forum
- Class GI. trial
