Private publisher access
GLP-1 Weight Loss Affiliate Programs
Clinician-led weight-management programs involving GLP-1 medicines where clinically appropriate.
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Apply for Private Telehealth AccessPrivate network · Publisher approval required
Find telehealth affiliate programs by the care topic your audience is researching. Explore the categories below, then apply for publisher access through MarketHealth.
Programs are available through private publisher review. Advertiser names, payouts, campaign materials and tracking links are shared only after the relevant approval. One publisher application starts the conversation; each campaign has its own requirements.
Private publisher access
Clinician-led weight-management programs involving GLP-1 medicines where clinically appropriate.
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Medical weight-management consultations and ongoing care, including programs beyond a single drug class.
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Telehealth program opportunities for publishers covering semaglutide-related weight-management care.
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Telehealth program opportunities for publishers covering tirzepatide-related weight-management care.
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Clinician-led testosterone evaluation and care programs for eligible adult patients.
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Private publisher programs involving online erectile-dysfunction consultations and clinician-directed care.
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Telehealth evaluation and care topics for adults seeking help with premature ejaculation.
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Men’s reproductive-health consultations, testing and clinician-reviewed fertility services.
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Menopause, perimenopause and clinician-directed hormone-care programs.
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Clinician-led consultations addressing adult women’s sexual-health concerns.
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Online contraception consultations and prescription services where available.
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Clinician-led assessment and ongoing care services for people seeking PCOS support.
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Online hair-loss evaluation and care options for eligible adults.
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Hair-loss consultations and clinician-directed programs intended for adult men.
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Hair-thinning consultations and clinician-directed programs intended for adult women.
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Virtual skin-care consultations across advertiser-approved dermatology services.
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Online acne consultations and clinician-directed skin-care plans.
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Virtual consultations and care programs for people seeking rosacea evaluation.
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Clinician-reviewed prescription skin-care programs for advertiser-approved concerns.
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Online mental-health evaluation and ongoing care services within each advertiser’s clinical scope.
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Clinician-led sleep consultations and care services.
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Online migraine evaluation and clinician-directed care programs.
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Laboratory-testing programs with clearly defined ordering, collection and results services.
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Clinician-led memberships, consultations and testing services focused on healthy-aging interests.
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Licensed clinical programs involving peptide-related care where the specific product and use are currently permissible.
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A private publisher inquiry category for clinician-led programs involving sermorelin, subject to formulation and campaign review.
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Private publisher inquiries for clinician-led glutathione service programs, subject to campaign review.
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Private publisher inquiries for clinician-led NAD+ service programs.
Apply for AccessPeptide medicines, compounded preparations and research products have different requirements. This directory does not advertise research-use-only products as treatments or imply that a trending substance is available through a permissible clinical program.
NAD+ appears as an adjacent clinical-wellness topic; it is not a peptide.
This is a topic directory for prospective publishers, not a ranking by sales, search volume or payout. Clinical decisions belong to licensed healthcare professionals.
Complete requested topic list · 31 entries
All 31 requested peptide and related telehealth names are listed below. Private program, publisher-review and investigational information pages have different scopes. A listing does not establish treatment availability, FDA approval or permission to promote.
01 · Private program page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →02 · Private program page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →03 · Product-specific private publisher review
Liraglutide has product-specific U.S. prescribing information. A named approved medicine does not make every preparation, indication or marketing claim equivalent. The private brief must identify the actual product and service.
View publisher information →04 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →05 · Product-specific private publisher review
PT-141 is listed here with the requested bremelanotide name. Vyleesi prescribing information concerns a specific bremelanotide product and use; it does not establish approval for every product marketed as PT-141.
View publisher information →06 · Investigational information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →07 · Investigational information — no treatment offer
Cagrilintide is an investigational topic. This page presents research-status information, not an available treatment-referral offer. Keep a single candidate separate from the CagriSema combination.
View publisher information →08 · Investigational information — no treatment offer
Novo Nordisk describes CagriSema as an investigational combination of cagrilintide and semaglutide. It is not the same entry as semaglutide alone or cagrilintide alone. This page does not present an available treatment offer.
View publisher information →09 · Investigational information — no treatment offer
Survodutide is covered as a clinical-development topic. Sponsor trial reporting does not establish a current MarketHealth treatment campaign or permission to promote the candidate to patients.
View publisher information →10 · Investigational information — no treatment offer
Altimmune identifies pemvidutide as investigational. This resource explains publisher coverage boundaries and does not advertise an approved product, a consumer purchase or an available treatment-referral campaign.
View publisher information →11 · Investigational information — no treatment offer
VK2735 is covered under its development code. A sponsor’s clinical-program announcement is not evidence of an approved medicine or an open treatment-referral offer. Keep the candidate distinct from approved products.
View publisher information →12 · Investigational information — no treatment offer
Novo Nordisk uses zenagamtide for the candidate formerly known as amycretin. These names share one information entry here. The candidate is covered as a development topic, not an available treatment-referral campaign.
View publisher information →13 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →14 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →15 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →16 · Publisher-review information
This entry preserves the explicit “with DAC” qualifier. It is separate from Modified GRF 1-29 and from the generic CJC-1295 topic. The exact advertiser preparation must be identified before any product or campaign description is approved.
View publisher information →17 · Publisher-review information
This entry preserves Modified GRF 1-29 and the requested “CJC-1295 without DAC” wording for identification. It is not merged with the with-DAC entry. A marketing alias does not substitute for precise product documentation.
View publisher information →18 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →19 · Publisher-review information
AOD-9604 has its own publisher-review entry. Interest in the name does not establish an approved weight-management indication or a currently permissible preparation. The proposed product and campaign need their own documentation.
View publisher information →20 · Publisher-review information
Thymosin Alpha-1 is kept separate from TB-500 and other thymosin-related names. This page makes no immune-treatment claim and does not infer campaign eligibility from a related substance or a historical list change.
View publisher information →21 · Publisher-review information
Epitalon is a distinct publisher-review topic. A longevity-oriented search or campaign nickname does not substantiate a lifespan, age-reversal or clinical-treatment promise. Any proposed description must match a reviewed preparation.
View publisher information →22 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →23 · Publisher-review information
KPV is retained as a separate requested topic. A short sequence or abbreviation does not establish product identity, route, permissible marketing or a treatment indication. The campaign brief must resolve those details.
View publisher information →24 · Publisher-review information
DSIP is listed as its own publisher-review topic. The abbreviation must not become a promise about sleep, sedation or treatment. Obtain the actual substance and proposed preparation before evaluating a campaign.
View publisher information →25 · Publisher-review information
Selank inquiries require an exact product record. Do not treat an alternate formulation or salt as automatically interchangeable, or turn a topic listing into an anxiety-treatment or cognitive-performance claim.
View publisher information →26 · Publisher-review information
Semax has a separate information page from Selank. Similar audience interest does not make two named substances equivalent or establish a permissible cognitive or neurological treatment campaign.
View publisher information →27 · Publisher-review information
GHRP-2 and GHRP-6 remain separate entries. Do not infer equivalent formulations, campaign terms or performance claims from the shared GHRP naming pattern. The actual proposed preparation must be reviewed.
View publisher information →28 · Publisher-review information
GHRP-6 is not combined with GHRP-2 in this directory. A related name does not establish the same product, clinical scope or publisher permissions. Review its own documentation before developing a campaign.
View publisher information →29 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →30 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →31 · Publisher review information page
Existing page retained; current program and preparation permissions remain subject to review.
View publisher information →CJC-1295 with DAC and Modified GRF 1-29 are separate entries. Amycretin and Zenagamtide share one identity entry. Blend names do not establish ingredients or an approved indication.
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