★ Metabolic Longevity

Thymosin Alpha-1

Metabolic Longevity · 2mg × 10 vials

In plain terms: Thymosin Alpha-1 is a research compound - oral, long-acting and well studied.

✓ 98%+ Purity ✓ Lab Tested ✓ COA on Request ✓ Discreet Shipping ✓ Direct Support
📋 Certificate of Analysis Request the third-party COA via Telegram
Quick Start
🧪
Format
Injectable (reconstituted) · 2mg × 10 vials
🎯
Who it's for
long-COVID
💉
How it's run
1.6 mg SubQ
When you'll notice
2-4 weeks
Pricing
$100from · kit of 10
US: 2-5 day · Intl: 7-14 day
+ $40 ship · singles $20 · free over $1k per tier
2mg × 10 vials$100
5mg × 10 vials$170
10mg × 10 vials$305
Order / Consult on Telegram →
~2 hr (plasma); biological effects persist days-to-weeks via T-cell maturation
Half-life
continuous
Cycling
2-4 weeks
First effects
metabolic-longevity
Class
Overview

What Is Thymosin Alpha-1?

Thymosin Alpha-1 is a 28-amino-acid peptide naturally produced by the thymus, the gland that "trains" T-cells. As people age (and especially during chronic infection, sepsis, cancer, or post-viral syndromes like long-COVID), thymic output collapses and naive T-cell production tanks. Tα1 acts as a thymic replacement signal: it pushes immature thymocytes through maturation into functional CD4+ and CD8+ T-cells, activates natural killer (NK) cells and dendritic cells, and upregulates Toll-like receptor signaling (primarily TLR9 and TLR2) on antigen-presenting cells. Net effect is a rebalancing of immune function, it pushes a depressed immune system back toward competent Th1-style response (cell-mediated, antiviral, antitumor) while simultaneously dampening the runaway inflammation seen in sepsis and cytokine storm. This dual action (boost where suppressed, calm where over-firing) is why the same molecule is used both for chronic viral hepatitis (where the immune system needs to wake up and clear the virus) and for sepsis/COVID ICU patients (where it needs to stop killing the host with cytokines). Approved as Zadaxin in 35+ countries for HBV, HCV, and as an immune adjuvant; in the US it remains research-use only.

Protocols

Typical dose ranges by experience level - educational reference. Message us and we tailor it to you.

Protocol1.6 mg SubQ
Frequency2× per week (Mon/Thu or similar 3-4 day spacing)
Duration8-12 weeks before assessing; many continuous-use protocols run indefinitely at this dose

This is the Zadaxin label dose for HBV/HCV and is the same dose used in most COVID-ICU trials. It's the universal starting point for long-COVID, chronic Lyme, post-viral fatigue, and immunocompromised support. Effect curve is slow: most users describe a subtle "lifting" of post-viral fatigue and brain fog around weeks 3-6, with more sustained energy by weeks 8-12. Don't expect a dramatic week-1 response.

Protocol1.6 mg SubQ, can push to 3.2 mg if no response at 12 weeks
Frequency2× per week at 1.6 mg, or 1.6 mg daily for 5-7 day acute pulses during active infection / flare
DurationContinuous or block-cycle (8 weeks on / 4 off) for chronic users. Acute infection pulses are 5-14 days.

Intermediate band is for users who've run the standard protocol 8-12 weeks and want to push harder, or who are stacking for an active immune challenge (chronic Lyme, mold illness, EBV reactivation, post-COVID flare). Some practitioners (Patterson protocol for long-COVID) pulse Tα1 alongside maraviroc/statin combos at this intermediate intensity. Stacks well at this band with LL-37 for active infection and NAD+ for mitochondrial recovery.

Protocol3.2-6.4 mg SubQ, sometimes split AM/PM
FrequencyDaily for short acute windows (5-14 days), or 3× per week for sustained advanced protocols
DurationAcute pulse 1-2 weeks for active infection / post-surgical immune support / cancer-adjunctive cycles. Sustained advanced use 12-24 weeks.

Advanced dosing is used in oncology adjunctive settings (typically alongside chemo cycles, dosed on the days around treatment to preserve immune function), in HBV/HCV combo protocols (with interferon or DAAs), and in sepsis / severe acute infection. Outside those acute clinical contexts, advanced dosing is rarely necessary for outpatient immune support. The 6.4 mg/day signal comes from sepsis trial protocols, not from chronic outpatient use. If a customer is asking about advanced dosing for chronic fatigue or long-COVID, the right answer is almost always "stay at 1.6 mg 2x/wk longer and add NAD+/MOTS-c" rather than push the dose.

What To Expect
2-4 weeks
Subjective immune/energy shift
8-12 weeks
Measurable t-cell/nk changes
Side Effects

Straight talk - what people actually report, and what the studies measured.

What users report
From forums, Discord & TikTok
  • Mild fatigue / "immune flare" in week 1-2: some users describe a brief "feeling like getting sick" sensation as the immune system reactivates, resolves on its own
  • Injection site stinging: more often reported on abdomen, less on thigh
  • Subtle effect: most common complaint is that effects are too subtle to feel; long-COVID users in particular report the benefit shows up as "I didn't crash this month" rather than as a dramatic energy surge
  • Vivid dreams / sleep changes: occasional report, not consistent
  • "Lyme/mold herx" (Jarisch-Herxheimer-like response): some chronic-infection users report a transient flare in symptoms in the first 2-3 weeks, attributed to immune reactivation against latent infection; usually resolves and is interpreted as a working signal
  • - Divergence: Clinical trials show essentially no symptom burden from Tα1 alone; community in chronic Lyme/long-COVID contexts reports a real herx-like response in week 1-3 in ~15-25% of users. This is a population-effect (sick population reactivating immunity), not a drug toxicity, and is generally taken as a positive sign that the peptide is doing something.
What the studies show
Measured in clinical trials
  • Injection site reactions (erythema, mild discomfort): 5-10% - mild, transient, no treatment-limiting cases
  • Headache: 3-5% - mild
  • Fatigue (transient): 2-4% - generally first 1-2 weeks then resolves
  • Flu-like symptoms (low-grade): occasional, particularly when combined with interferon in HCV protocols - attributable mainly to interferon
  • Serious adverse events (in HBV/HCV and sepsis trials): no significant safety signal across thousands of patients in 30+ years of clinical use; the WHO and EMA safety database flags no consistent serious AE
  • Hypersensitivity: rare, <1%
  • Lab signal: no consistent hepatic, renal, or hematologic toxicity in trials. Tα1 has one of the cleanest safety profiles in the peptide research space.
The Research

Peer-reviewed studies and clinical guidelines - tap any to read the source.

PubMedGoldstein et al, From lab to bedside: emerging clinical applications of thymosin alpha 1 (PMC2750086)

](https://pmc.ncbi.nlm.nih.gov/articles/PMC2750086/) - comprehensive mechanism + clinical applications review by the discoverer of Tα1

Read study ↗
PubMedCamerini & Garaci, Historical review on the discovery of thymosin alpha 1 (PMC4859321)

](https://pmc.ncbi.nlm.nih.gov/articles/PMC4859321/) - discovery history, T-cell maturation mechanism, regulatory approvals across 35+ countries

Read study ↗
PubMedThymosin alpha 1 therapy in chronic hepatitis B, meta-analysis (PMID 11737030)

](https://pubmed.ncbi.nlm.nih.gov/11737030/) - HBV response rates ~25-40% sustained virologic response vs ~10-15% untreated controls

Read study ↗
PubMedThymosin alpha 1 in HCV combination therapy (PMC3539291)

](https://pmc.ncbi.nlm.nih.gov/articles/PMC3539291/) - HCV combination data with interferon and ribavirin

Read study ↗
PubMedLiu et al, Thymosin Alpha 1 reduces 28-day mortality in severe sepsis (PMID 23979484)

](https://pubmed.ncbi.nlm.nih.gov/23979484/) - RCT, Tα1 reduced sepsis 28-day mortality from 35% to 26% (absolute reduction 9%, p=0.06 trending)

Read study ↗
PubMedWei Liu et al, Thymosin alpha 1 reduces mortality in severe COVID-19 (Clin Infect Dis 2020, PMC7184460)

](https://pmc.ncbi.nlm.nih.gov/articles/PMC7184460/) - retrospective cohort, 76 severe COVID patients, Tα1 reduced 28-day mortality from 30% to 11%

Read study ↗
+ 7 more studies & references
From The Community

Aggregated sentiment from public forums & socials - real-world reports, not individual endorsements.

Rr/Peptides Tα1 mega-th

Mild fatigue / "immune flare" in week 1-2: some users describe a brief "feeling like getting sick" sensation as the immune system reactivates, resolves on its own

Rr/covidlonghaulers Tα1

Injection site stinging: more often reported on abdomen, less on thigh

Rr/Lyme thymosin alpha-

Subtle effect: most common complaint is that effects are too subtle to feel; long-COVID users in particular report the benefit shows up as "I didn't crash this month" rather than as a dramatic energy surge

PPeptide Sciences Tα1 p

Vivid dreams / sleep changes: occasional report, not consistent

Rr/Peptides Tα1 mega-th

"Lyme/mold herx" (Jarisch-Herxheimer-like response): some chronic-infection users report a transient flare in symptoms in the first 2-3 weeks, attributed to immune reactivation against latent infection; usually resolves and is interpreted as a working signal

Rr/covidlonghaulers Tα1

- Divergence: Clinical trials show essentially no symptom burden from Tα1 alone; community in chronic Lyme/long-COVID contexts reports a real herx-like response in week 1-3 in ~15-25% of users. This is a population-effect (sick population reactivating immunity), not a drug toxicity, and is generally taken as a positive sign that the peptide is doing…

Common Questions
SubQ injection (the FDA Zadaxin label is SubQ; IV has been used in ICU trials but is not standard for outpatient use). 1.6 mg SubQ
2-4 weeks for subjective immune/energy shift; 8-12 weeks for measurable T-cell/NK changes
A popular pairing is Tα1 + BPC-157. See the Protocols section, or ask us for a stack built around your goal.
Yes. Every batch is third-party lab tested - request the COA on Telegram and we send it over.
Safety & Contraindications

Hard stops

  • Active solid organ transplant on immunosuppressants (Tα1 directly opposes immunosuppression, can trigger rejection)
  • Known hypersensitivity to thymosin peptides
  • Active autoimmune flare being actively immunosuppressed (relative contraindication, see Caution below)

Caution flags

  • Autoimmune disease (Hashimoto's, lupus, RA, MS, psoriasis, type 1 diabetes): Tα1 is an immune modulator, not a pure stimulant, but the theoretical risk of pushing toward Th1 response can flare autoimmune disease in a subset of users. Start low (1.6 mg 1x/wk, ramp to 2x/wk if tolerated), watch for symptom flare in weeks 2-4.
  • Pregnancy / breastfeeding (no data, default contraindication)
  • Active cancer being managed without medical oversight (Tα1 is used adjunctively with conventional cancer treatment, not as a substitute, and self-administration outside a treatment context is not advised)
  • Severe immunodeficiency from genetic causes (HIV not a contraindication, may be beneficial; primary immunodeficiencies are unknown territory)

Stacking conflicts

  • Active immunosuppressants (cyclosporine, tacrolimus, methotrexate, biologics like adalimumab/rituximab) - pharmacologic conflict
  • High-dose steroids - pharmacologic conflict at the immune-suppression layer; low-dose intermittent steroid use is fine
Is It Right For You?

✓ Good fit

  • long-COVID
  • chronic Lyme
  • post-viral fatigue
  • chronic HBV/HCV support
  • immunocompromised over 60
  • post-cancer maintenance
  • frequent infections
  • post-surgical immune support
  • EBV reactivation
  • mold illness / CIRS

✗ Not a fit

  • active autoimmune flare on immunosuppressants
  • organ transplant recipients
  • customers wanting a same-week energy/performance boost
  • pregnant/breastfeeding

Administration & Storage

Route: SubQ injection (the FDA Zadaxin label is SubQ; IV has been used in ICU trials but is not standard for outpatient use)

Injection site: abdomen, outer thigh, or back of upper arm; rotate sites. Some users report less injection-site stinging on the thigh vs abdomen.

Storage: refrigerated, ~14-28 days after reconstitution. Tα1 is more stable than BPC/TB but still degrades, don't keep a reconstituted vial past a month. Unreconstituted lyophilized powder is shelf-stable at room temp for short windows but should be refrigerated for long storage.

Notes: Zadaxin label dosing is 1.6 mg twice weekly with at least 3-4 days between doses (typical pattern: Monday + Thursday, or Tuesday + Friday). Inject on consistent days. No need to time around meals. Some clinical protocols (sepsis, COVID-ICU) used daily dosing at 1.6-3.2 mg for short acute windows, but outpatient/chronic use is always the 2x/wk pattern.

All products sold for research purposes only. Not for human or animal consumption. Must be 21 or older to purchase. By placing an order you confirm compliance with all applicable local laws and regulations.