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Specimen Atlas of Research Peptides30 plates · MIT
Side-by-side · Research reference

LiraglutidevsTesofensine

Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.

AFDA-ApprovedVerified14/45 cited
BPhase 3Draft10/40 cited
Liraglutide
Daily GLP-1 RA · FDA-Approved
SQ · Abdomen / thigh / arm · Once daily
Tesofensine
SNDRI · Phase 3 obesity candidate
0.25–0.5 mgDaily doseAstrup 2008
9.2 kgWeight ↓ (24 wk)Astrup 2008
Phase 3Evidence levelAstrup 2008
Oral · Once daily morning

01Mechanism of Action

Parameter
Liraglutide
Tesofensine
Primary target
Serotonin / norepinephrine / dopamine transporters (SERT / NET / DAT)Astrup 2008
Pathway
GLP-1R agonism → ↑glucose-dependent insulin, ↓glucagon, ↓gastric emptying, ↓appetiteSAXENDA (liraglutide) injectio 2014Marso 2016
Triple monoamine reuptake inhibition → ↑synaptic 5-HT, NE, DA → appetite suppression + thermogenesisAstrup 2008
Downstream effect
Glycemic improvement, modest body-weight reduction, cardiovascular event reduction in high-risk T2DMarso 2016
Strong appetite suppression, mild thermogenic effect, weight lossAstrup 2008
Feedback intact?
Glucose-dependent insulin release preserves physiological feedback
Origin
Modified GLP-1(7-37) with Lys26 substitution (Arg34) and C-16 palmitoyl-glutamate acylation for albumin bindingSAXENDA (liraglutide) injectio 2014
Small molecule developed by NeuroSearch (Denmark) for CNS indications, repurposed for obesityAstrup 2008
Antibody development

02Dosage Protocols

Parameter
Liraglutide
Tesofensine
Standard dose (T2D, Victoza)
Standard dose (weight, Saxenda)
3.0 mg / day (after 5-week titration)SAXENDA (liraglutide) injectio 2014
Frequency
Once daily, same time each day
Once daily, morning
Titration schedule
0.6 → 1.2 → 1.8 → 2.4 → 3.0 mg over 5 weeks
Mitigates GI side effects.
Evidence basis
FDA-approved · Phase 3 RCTs (LEADER, SCALE)Marso 2016SAXENDA (liraglutide) injectio 2014
Phase 2b + ongoing Phase 3Astrup 2008
Duration
Indefinite for chronic indication
24 weeks per studied cycle
Reconstitution
Pre-filled commercial pen (no reconstitution)
Timing
Any time of day; consistent
Morning to avoid sleep disruption
Half-life
~9 days (very long)
Standard dose
0.25–0.5 mg / dayAstrup 2008
Lower / starter dose
0.125 mg / day
Form
Oral capsule

04Side Effects & Safety

Parameter
Liraglutide
Tesofensine
GI symptoms
Nausea, vomiting, diarrhea (very common during titration)SAXENDA (liraglutide) injectio 2014
Pancreatitis risk
Rare; discontinue if suspected
Thyroid C-cell tumours
Boxed warning — contraindicated in MEN2 / MTC historySAXENDA (liraglutide) injectio 2014
Hypoglycemia
Low risk as monotherapy; elevated with sulfonylureas / insulin
Heart rate
Modest ↑ resting HR (~2-3 bpm)
Cardiovascular benefit
↓ MACE in high-risk T2D (LEADER trial)Marso 2016
Pregnancy / OB
Contraindicated
Contraindicated
Heart rate / BP
Dose-dependent ↑ HR + BPAstrup 2008
Insomnia
Dose-related; mitigate with morning timing
Dry mouth
Common
Nausea
Common
Mood changes
Anxiety / agitation possible
Cardiovascular events
Phase 3 trial monitoring; not yet FDA-cleared
Absolute Contraindications
Liraglutide
  • ·MTC personal or family history; MEN2
  • ·Pregnancy / breastfeeding
  • ·Hypersensitivity to liraglutide
Tesofensine
  • ·Pregnancy / breastfeeding
  • ·Severe cardiovascular disease
  • ·Concurrent MAOI use
Relative Contraindications
Liraglutide
  • ·Severe gastroparesis
  • ·History of pancreatitis
  • ·Severe gastrointestinal disease
Tesofensine
  • ·Hypertension
  • ·Anxiety disorder
  • ·Insomnia

05Administration Protocol

Parameter
Liraglutide
Tesofensine
1. Reconstitution / device
Commercial pre-filled pen, no reconstitution required.
Oral capsule (investigational; not commercial).
2. Injection site
SQ — abdomen, thigh, or upper arm. Rotate sites.
Swallow whole with water, morning only.
3. Timing
Once daily, same time each day. Take with or without food.
Morning to mitigate insomnia. Do not dose evening.
4. Storage
Refrigerate 2–8 °C unopened; room temp ≤30 °C up to 30 days after first use.
Room temp ≤25 °C, dry place.
5. Needle
Pen-supplied 32G needle.
Monitor BP + HR + mood. Avoid stimulants + MAOIs.