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Thymalfasin API from Indian Manufacturers & Suppliers

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Producer
Produced in  China
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Employees: 373

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MSDS
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CoA
Producer
Produced in  China
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Employees: 1000+

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Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
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USDMF
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MSDS
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BSE/TSE
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CoA

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Producer
Produced in  India
|

Employees: 200+

|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
|
MSDS
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BSE/TSE
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CoA

All certificates

GMP
MSDS
BSE/TSE
CoA
Producer
Produced in  China
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Employees: 1500+

|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
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MSDS
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BSE/TSE
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CoA

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CoA
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coa
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Certifications: USDMF
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CoA

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USDMF
CoA
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Thymalfasin | CAS No: 62304-98-7 | GMP-certified suppliers

A medication that supports improved immune responses to influenza and hepatitis B vaccination in older adults and hemodialysis patients with inadequate prior immunization.

Therapeutic categories

Adjuvants, ImmunologicAmino Acids, Peptides, and ProteinsAntineoplastic AgentsHormonesHormones, Hormone Substitutes, and Hormone AntagonistsImmunologic Factors
Generic name
Thymalfasin
Molecule type
biotech
CAS number
62304-98-7
DrugBank ID
DB04900
Approval status
Investigational drug

Primary indications

  • Indicated as an adjuvant for influenza vaccine in elderly patients and as an adjuvant for both influenza and hepatitis B vaccines in chronic hemodialysis patients who failed to achieve adequate antibody titers from previous immunization

Product Snapshot

  • Thymalfasin is an injectable peptide supplied as a lyophilized powder for intramuscular or subcutaneous administration
  • It is used as an immunomodulatory adjuvant to enhance vaccine response in elderly populations and in hemodialysis patients with inadequate antibody titers to influenza or hepatitis B vaccination
  • It is currently investigational with no FDA or EMA marketing approval

Clinical Overview

Thymalfasin (CAS 62304-98-7) is a synthetic form of thymosin alpha 1, an acetylated 28‑amino‑acid polypeptide identical to the endogenous human sequence. It is used internationally for immunomodulatory applications and is approved in several countries for management of chronic hepatitis B and C. Current investigated indications include use as an adjuvant to enhance vaccine responses. It is indicated as an adjunct to influenza vaccination in older adults and as an adjuvant to influenza and hepatitis B vaccines in hemodialysis patients with inadequate antibody titers after prior immunization.

Thymalfasin exhibits pharmacodynamic activity focused on T‑cell–mediated immunity. In vitro studies show enhanced T‑cell differentiation and maturation with increases in CD3+, CD4+, and CD8+ subsets. It stimulates production of Th1‑type cytokines including interferon gamma and interleukin‑2 and promotes expression of the interleukin‑2 receptor following activation. Additional findings include increased natural killer cell cytotoxicity, enhanced responses to T‑cell‑dependent antigens, and protection of thymocytes from dexamethasone‑induced apoptosis. Upregulation of toll‑like receptors such as TLR2 and TLR9 in dendritic cells and activation of NF‑kB and JNK/P38/AP1 signaling pathways provide further mechanistic context for its immunomodulatory and antiviral effects.

The mechanism of action is not fully defined but is broadly attributed to augmentation of cellular immune function, including effects on thymocyte maturation and activation of pluripotent precursor cells. In vivo animal models demonstrate protective effects against chemotherapy‑ or irradiation‑induced immunosuppression and reduced susceptibility to opportunistic infections, though these findings are model‑specific.

Absorption, distribution, metabolism, and excretion characteristics are not comprehensively defined in clinical literature. Safety experience reflects its use as an immunomodulator, with attention to immune activation effects and the need for monitoring in populations with altered immune status.

For API procurement, sourcing should prioritize manufacturers with demonstrated control of peptide synthesis, impurity profiles, and consistency of sequence fidelity, as well as robust quality documentation aligned with global regulatory expectations.

Identification & chemistry

Generic name Thymalfasin
Molecule type Biotech
CAS 62304-98-7
UNII W0B22ISQ1C
DrugBank ID DB04900

Pharmacology

SummaryThymalfasin is a synthetic 28‑amino‑acid peptide that modulates immune function primarily through enhancing T‑cell differentiation, maturation, and activation. It promotes Th1‑type cytokine production, augments natural killer cell activity, and influences dendritic cell signaling pathways such as TLR2/TLR9 and NF‑kB. These coordinated actions support its use as an immunologic adjuvant to improve vaccine responsiveness.
Mechanism of actionThe mechanism of action of thymalfasin is not completely understood but is thought to be related to its immunomodulating activities, centered primarily around augmentation of T-cell function. In various in vitro assays, thymosin alpha 1 has been shown to promote T-cell differentiation and maturation; for example, CD4+, CD8+, and CD3+ cells have all been shown to be increased. Thymosin alpha 1 has also been shown to increase production of IFN-g, IL-2, IL-3, and expression of IL-2 receptor following activation by mitogens or antigens, increase NK cell activity, increase production of migratory inhibitory factor (MIF), and increase antibody response to T-cell dependent antigens. Thymosin alpha 1 has also been shown to antagonize dexamethasone-induced apoptosis of thymocytes in vitro. In vivo administration of thymosin alpha 1 to animals immunosuppressed by chemotherapy, tumor burden, or irradiation showed that thymosin alpha 1 protects against cytotoxic damage to bone marrow, tumor progression and opportunistic infections, thereby increasing survival time and number of survivors. Many of the in vitro and in vivo effects of thymosin alpha 1 have been interpreted as influences on either differentiation of pluripotent stem cells to thymocytes or activation of thymocytes into activated T-cells. Thymalfasin also has been shown in vitro to upregulate expression of toll like receptors (TLR) including TLR2 and TLR9 in mouse and human dendritic cells, as well as activate NF-kB and JNK/P38/AP1 pathways. Thymalfasin's activation of dendritic cells provides another possible pathway explaining thymalfasin's immunomodulatory and antiviral effects.
PharmacodynamicsThymalfasin is a 28-amino acid polypeptide produced synthetically but originally isolated from thymosin fraction 5, a bovine thymus extract containing a number of immunologically active peptides. In vitro studies have shown that Thymalfasin can influence T-cell production and maturation, stimulate production of Th1 cytokines such as interferon-gamma and interleukin-2, and activate natural killer cell-mediated cytotoxicity.

ADME / PK

AbsorptionRapidly absorbed with peak serum levels achieved at approximately 2 hours.
Half-lifeApproximately 2 hours. There is no evidence of accumulation following multiple subcutaneous doses.

Formulation & handling

  • Lyophilized peptide requires reconstitution with suitable diluent and protection from proteolytic degradation during processing and storage.
  • Formulated exclusively for parenteral use (IM/SC), with sensitivity to thermal stress and moisture necessitating low‑temperature, low‑humidity handling.
  • As a biotech peptide, adsorption to surfaces and oxidation should be controlled through appropriate container materials and antioxidant or stabilizing excipients.

Regulatory status

Safety

ToxicityThere are no reported instances of deliberate or accidental overdosage in humans. Animal toxicology studies have shown no adverse reactions in single doses up to 20 mg/kg and in repeated doses up to 6 mg/kg/day for 13 weeks, which were the highest doses studied. The highest single dose tested in animals represents 800-times the clinical dose.
High Level Warnings:
  • Animal studies showed no adverse reactions at single doses up to 20 mg/kg or repeated doses up to 6 mg/kg/day for 13 weeks, indicating a wide toxicological safety margin relative to clinical exposure
  • The highest single dose evaluated in animals (20 mg/kg) was approximately 800-fold higher than the human clinical dose, with no dose-limiting toxicities observed
  • No documented cases of human overdosage have been reported, and available data do not indicate acute toxicity concerns under intended handling and manufacturing conditions

Thymalfasin is a type of Immunostimulants


Immunostimulants are a vital subcategory of pharmaceutical active pharmaceutical ingredients (APIs) that play a crucial role in bolstering the immune system. These substances, also referred to as immunomodulators, are designed to enhance the body's natural defense mechanisms and promote a more robust immune response. Immunostimulants are widely used in the development of drugs and vaccines, particularly for the treatment and prevention of infectious diseases.

These pharmaceutical compounds work by activating various components of the immune system, such as macrophages, natural killer cells, and T-cells. By stimulating these immune cells, immunostimulants help in improving the body's ability to recognize and eliminate pathogens, thereby reducing the risk of infection and enhancing overall health.

Immunostimulants can be derived from various sources, including synthetic chemicals, plant extracts, and biological agents. Examples of commonly used immunostimulants include interferons, interleukins, and Toll-like receptor (TLR) agonists. These substances can be administered through different routes, such as oral ingestion, injection, or topical application, depending on the desired therapeutic effect.

Pharmaceutical companies invest significant resources in the research and development of immunostimulant APIs due to their potential to revolutionize disease management. By harnessing the power of the immune system, these APIs offer promising solutions for various medical conditions, including viral infections, cancer, and autoimmune disorders.

In conclusion, immunostimulants are a critical subcategory of pharmaceutical APIs that stimulate the immune system to enhance its defense mechanisms. Their use holds great potential in the prevention and treatment of various diseases, making them an essential focus for pharmaceutical research and development.


Thymalfasin (Immunostimulants), classified under Immunomodulators


Immunomodulators, a category of pharmaceutical active pharmaceutical ingredients (APIs), are substances that help regulate and modify the immune response of an individual. These compounds play a crucial role in treating various immune-related disorders and diseases. Immunomodulators work by either enhancing or suppressing the immune system, depending on the specific condition being treated.

Immunomodulators are used in the treatment of autoimmune disorders, such as rheumatoid arthritis, multiple sclerosis, and psoriasis. By suppressing the immune system, these APIs help reduce the overactive immune response associated with these conditions, thereby alleviating symptoms and preventing further damage to the body's tissues.

On the other hand, immunomodulators are also employed to boost the immune system in cases of immunodeficiency disorders. These APIs stimulate the immune response, enabling the body to better fight off infections and diseases. Additionally, immunomodulators are utilized in the prevention and treatment of organ transplant rejection, where they help modulate the immune system to accept the transplanted organ.

The development and production of immunomodulators require rigorous testing and quality control to ensure their safety and efficacy. Pharmaceutical companies carefully formulate these APIs into various dosage forms, including tablets, capsules, injections, and topical preparations, to cater to different patient needs.

In summary, immunomodulators form a vital category of pharmaceutical APIs that regulate and modify the immune system. With their ability to modulate immune responses, these compounds contribute significantly to the management and treatment of various immune-related disorders and diseases, improving the quality of life for many patients.



Thymalfasin API manufacturers & distributors

Compare qualified Thymalfasin API suppliers worldwide. We currently have 6 companies offering Thymalfasin API, with manufacturing taking place in 3 different countries. Use the table below to review supplier type, countries of origin, certifications, product portfolio and GMP audit availability.

SupplierTypeCountryProduct originCertificationsPortfolio
Producer
China China BSE/TSE, CoA, GMP, MSDS33 products
Producer
India India BSE/TSE, CoA, GMP, MSDS166 products
Producer
China China CoA11 products
Producer
China China BSE/TSE, CoA, GMP, MSDS, USDMF34 products
Producer
Sweden Unknown CoA, USDMF21 products
Producer
China China BSE/TSE, CoA, EDMF/ASMF, GMP, JDMF, KDMF, MSDS, USDMF25 products

When sending a request, specify which Thymalfasin API quality you need: for example EP (Ph. Eur.), USP, JP, BP, or another pharmacopoeial standard, as well as the required grade (base, salt, micronised, specific purity, etc.).

Use the list above to find high-quality Thymalfasin API suppliers. For example, you can select GMP, FDA or ISO certified suppliers. Visit our help page to learn more about sourcing APIs via Pharmaoffer.

Frequently asked questions about Thymalfasin API


Sourcing

Which documents are typically required when sourcing Thymalfasin API?
Request the core API documentation set: CoA (5 companies), GMP (3 companies), MSDS (3 companies), BSE/TSE (3 companies), USDMF (2 companies). Confirm versions and validity dates match the destination market to avoid delays in qualification.
Which manufacturers are known to produce Thymalfasin API?
Known or reported manufacturers for Thymalfasin: Chengdu Shengnuo Biopharm Co., Ltd., Suzhou Tianma Pharma Group Tianji Bio-Pharmaceutical Co., Ltd, Gonane Pharma. Evaluate their GMP history, scale, and regional coverage before requesting dossiers or allocating demand.
How can I request quotes for Thymalfasin API from GMP suppliers?
Submit quote requests through the supplier listings with your specs and required documents (specifications, target volume, delivery timeline, and destination). Providing consistent details upfront speeds comparable offers and clarifies technical feasibility.
Is a GMP audit report available for Thymalfasin manufacturers?
Audit reports may be requested for Thymalfasin: 0 GMP audit reports available. Confirm the scope and recency of any audit before relying on it for qualification decisions.
How many suppliers offer Thymalfasin API on Pharmaoffer?
Reported supplier count for Thymalfasin: 5 verified suppliers. Filter listings by certifications, regions, and delivery options to match your qualification plan.
Which countries are known to manufacture Thymalfasin API?
Production countries reported for Thymalfasin: China (3 producers), India (1 producer). Knowing the manufacturing geography helps anticipate logistics lead times and import compliance needs.
Which certifications do suppliers of Thymalfasin usually hold?
Common certifications for Thymalfasin suppliers: CoA (5 companies), GMP (3 companies), MSDS (3 companies), BSE/TSE (3 companies), USDMF (2 companies). Always verify issuing authorities and expiry dates when reviewing audit packages.

Technical

What is Thymalfasin (CAS 62304-98-7) used for?
Thymalfasin is used as an immunomodulator, primarily as adjunct therapy for chronic hepatitis B and C. It is also employed to enhance vaccine responses, including as an adjuvant to influenza vaccination in older adults and to influenza and hepatitis B vaccines in hemodialysis patients with inadequate antibody titers. Its use is based on its ability to augment T‑cell–mediated immunity and related cytokine activity.
Which therapeutic class does Thymalfasin fall into?
Thymalfasin belongs to the following therapeutic categories: Adjuvants, Immunologic, Amino Acids, Peptides, and Proteins, Antineoplastic Agents, Hormones, Hormones, Hormone Substitutes, and Hormone Antagonists. This positioning helps teams compare alternative APIs, anticipate pharmacology expectations, and align early research priorities.
What conditions is Thymalfasin mainly prescribed for?
The primary indications for Thymalfasin: Indicated as an adjuvant for influenza vaccine in elderly patients and as an adjuvant for both influenza and hepatitis B vaccines in chronic hemodialysis patients who failed to achieve adequate antibody titers from previous immunization. These use cases frame the target patient populations and help prioritize formulation and safety evaluations.
How does Thymalfasin work?
The mechanism of action of Thymalfasin is not completely understood but is thought to be related to its immunomodulating activities, centered primarily around augmentation of T-cell function. In various in vitro assays, thymosin alpha 1 has been shown to promote T-cell differentiation and maturation; for example, CD4+, CD8+, and CD3+ cells have all been shown to be increased. Thymosin alpha 1 has also been shown to increase production of IFN-g, IL-2, IL-3, and expression of IL-2 receptor following activation by mitogens or antigens, increase NK cell activity, increase production of migratory inhibitory factor (MIF), and increase antibody response to T-cell dependent antigens. Thymosin alpha 1 has also been shown to antagonize dexamethasone-induced apoptosis of thymocytes in vitro. In vivo administration of thymosin alpha 1 to animals immunosuppressed by chemotherapy, tumor burden, or irradiation showed that thymosin alpha 1 protects against cytotoxic damage to bone marrow, tumor progression and opportunistic infections, thereby increasing survival time and number of survivors. Many of the in vitro and in vivo effects of thymosin alpha 1 have been interpreted as influences on either differentiation of pluripotent stem cells to thymocytes or activation of thymocytes into activated T-cells. Thymalfasin also has been shown in vitro to upregulate expression of toll like receptors (TLR) including TLR2 and TLR9 in mouse and human dendritic cells, as well as activate NF-kB and JNK/P38/AP1 pathways. Thymalfasin's activation of dendritic cells provides another possible pathway explaining Thymalfasin's immunomodulatory and antiviral effects.
What should someone know about the safety or toxicity profile of Thymalfasin?
Thymalfasin has a wide toxicological safety margin in animal studies, with no adverse effects observed at single doses up to 20 mg/kg or repeated doses up to 6 mg/kg/day for 13 weeks. These exposures were many‑fold higher than human clinical doses and did not reveal dose‑limiting toxicities. No human overdosage cases have been reported, and available experience does not indicate acute toxicity concerns under intended handling and manufacturing conditions. Monitoring is generally focused on immunomodulatory effects, particularly in individuals with altered immune status.
What are important formulation and handling considerations for Thymalfasin as an API?
Thymalfasin is supplied as a lyophilized peptide that requires reconstitution with an appropriate diluent and protection from proteolytic degradation during processing and storage. It is intended only for parenteral administration, and its sensitivity to thermal stress and moisture necessitates low‑temperature, low‑humidity handling. Adsorption to surfaces and susceptibility to oxidation should be minimized by selecting suitable container materials and, when appropriate, stabilizing or antioxidant excipients.
Is Thymalfasin a biotech?
Thymalfasin is classified as a biotech. That classification shapes process design, impurity profiling, and analytical control strategies.
Are there special stability concerns for oral Thymalfasin?
Thymalfasin is formulated exclusively for parenteral use, so oral stability parameters are not applicable. As a lyophilized peptide, its known stability concerns relate to sensitivity to moisture, thermal stress, oxidation, and adsorption during processing and storage. These considerations apply to its intended injectable form rather than any oral formulation.

Pharmaoffer

How does Pharmaoffer’s Smart Sourcing Service help with Thymalfasin procurement?
Pharmaoffer's Smart Sourcing Service coordinates compliant suppliers, documentation, and competitive quotes for Thymalfasin. It centralizes outreach, follow-ups, and document validation to shorten procurement timelines.
Is Thymalfasin included in the PRO Data Insights coverage?
PRO Data Insights coverage for Thymalfasin: 13 verified transactions across 9 suppliers and 7 buyers worldwide. Use the dataset to benchmark suppliers and monitor regulatory activity where available.
Where can I access the API market report for Thymalfasin?
Market report availability for Thymalfasin: Report Available. The report highlights demand trends, pricing drivers, and supplier landscape insights for procurement planning.