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Thymosin Beta-4

Also called Tβ4, RGN-352

IntravenousEvidence B

Research reference

Research amount range
42–1260 mg per administration — not a starting amount
Reference frequency
Every day — catalogue input, not a personal schedule
Evidence route
Intravenous in the cited evidence; formulation matters.
Model accumulation timescale
~12.5 days — about five half-lives with regular repeated exposure; not time to a result
Storage
Storage and in-use limits depend on the exact formulation and packaging. A compound name alone cannot establish temperature, diluent, or shelf life. Details

A research and community reference, not medical advice. Figures are descriptive, vary between sources, and are not a recommendation for use.

When results may show

Thymosin Beta-4

Evidence gap
When change was measured
Human exposure or dose research exists for Thymosin Beta-4, but this catalogue has no source-backed window for a visible or functional result. Pharmacokinetic or biomarker timing is not the same as outcome timing.
When to assess
No evidence-based reassessment point is available for this catalogue entry. Half-life or clearance time cannot be used as a proxy for when a result should appear.
Conditions and limitations
No source-backed special condition—such as fasting, local injection, exercise timing, or a companion compound—has been established for the claimed outcomes. Route and formulation still matter.
When to stop
No validated target, maintenance phase, or quit rule is available. Do not extend or increase exposure solely because an expected result has not appeared; a severe or persistent reaction warrants stopping and prompt clinical review.

Research timing is descriptive, not a promise or personal instruction. A severe or persistent reaction needs prompt clinical review. This is not medical advice.

Thymosin β4 estimates vary widely; the TB-500 fragment page carries the same rough figure. Read as order-of-magnitude.

The full protein, distinct from the TB-500 fragment sold under that name. Human evidence is an intravenous safety study, so no subcutaneous schedule is established and no schedule table is shown; figures do not transfer to the fragment. The intravenous amounts studied (42–1260 mg) were infusions, not a vialled product, so the vial size shown is nominal — set just above the smallest studied amount so the calculator shows a possible single-vial draw rather than an impossible one.

Modelled level — every day

1× is the peak after a single dose.

Steady-state peak
4.13× single dose

Read off the modelled curve, not an even-interval formula

Time to steady state
12.5days

About five half-lives

Administrations
7/ week

Where these numbers come from

  • Ruff D et al., Ann N Y Acad Sci 2010;1194:223First-in-human intravenous thymosin β4 (RGN-352), single and 14-day daily doses across four ascending cohorts of 42, 140, 420 and 1260 mg, was assessed for safety in volunteers; no subcutaneous schedule was fixed.
  • Thymosin β4 preclinical repair literatureThe full protein's human data is limited to intravenous safety work; it is the parent molecule of the TB-500 fragment, and figures do not carry between the two.

Next steps

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