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Hydroxyprogesterone Caproate (OHPC)

Hydroxyprogesterone Caproate (OHPC)

Intramuscular Injection (IM)

Hydroxyprogesterone Caproate is a long-acting, injectable progestin. While it boasts a lengthy half-life, it is exceedingly rare in modern transgender HRT protocols. There is virtually zero clinical research regarding its safety or efficacy in transgender women. If you desire a progestogen, oral bioidentical micronized progesterone is infinitely preferred.


Hydroxyprogesterone Caproate (OHPC) is a synthetic derivative of 17α-hydroxyprogesterone, categorizing it as a semi-synthetic progestin [1] .

Core characteristics:

  • Administration: Mandatory Intramuscular (IM) injection. It cannot be taken orally.
  • Half-Life: Once injected deep into the muscle, it creates a depot effect lasting roughly 7 to 8 days.
  • Mechanism: It binds to the body’s progesterone receptors (PR), mimicking standard progestogenic activity.
  • Metabolism: Broken down heavily by the liver and excreted through the kidneys.
  • Global Branding: Previously famous as Makena (withdrawn from the US market in 2023) and Proluton (still accessible in gray markets and parts of Asia/EU).

The Difference from Bioidentical Progesterone

섹션 제목: “The Difference from Bioidentical Progesterone”
TratisMicronized ProgesteroneHydroxyprogesterone (OHPC)
Chemical Origin Bioidentical to human P4 Semi-synthetic derivative
Delivery Route Oral Softgel Intramuscular Injection
Frequency Daily Every 1 to 2 Weeks
Sedative Effect Yes (Heavy GABA-A interaction) None
GAHT Data Limited, but utilized broadly Non-existent
Tolerability High High rate of injection site pain

OHPC is a ghost in mainstream transgender medicine. The Endocrine Society 2017 Guidelines [2] and WPATH SOC 8 [3] completely ignore OHPC regarding gender-affirming care regimens.

Why would anyone use it?

  • A user suffers from extreme gastrointestinal intolerability to oral micronized progesterone.
  • A user fiercely desires a weekly injection rather than swallowing daily pills.
  • Deep gray market availability where bioidentical progesterone is geoblocked.

If utilized, OHPC functionally acts as a standard progestogen:

  • It theoretically could assist in lobuloalveolar breast maturation (Tanner IV-V), though there is not a single clinical trial proving this in trans women.
  • It indirectly assists in suppressing the HPG axis (lowering LH/FSH), gently aiding testosterone suppression.
  • It does not possess the anti-anxiety or sedative (sleep aid) properties that make oral progesterone massively popular.

ProtocolDosageAdministrationNotes
Standard OB/GYN Dose 250 mg / week Intramuscular Designed for cis women preventing miscarriage.
DIY Experimental Dose 125-250 mg / every 1-2 weeks Intramuscular Sourced from community self-reporting.

  • Severe Injection Site Reactions: OHPC is notoriously suspended in thick, painful carrier oils (like castor oil). Bruising, hard long-lasting lumps (indurations), and deep muscle aching are nearly guaranteed.
  • Nausea and Vertigo
  • Emotional Volatility: Like all progestogens, it can trigger severe, unprompted depressive episodes or PMS-like emotional crashes.
  • Anaphylaxis: Allergic reactions to the thick carrier oils are reported.

  • In the US: Functionally dead. The FDA ripped Makena (the premier OHPC brand) from the market in 2023 after investigations proved it did not actually help prevent preterm births.
  • The Grey Market: Brands like Proluton are still heavily trafficked by global DIY pharmacies operating out of regions with lax pharmaceutical export laws, making it accessible but difficult to verify for purity.

References

  1. Kuhl H. Pharmacology of estrogens and progestogens: influence of different routes of administration. Climacteric 2005;8(Suppl 1):3-63. DOI:10.1080/13697130500148875
  2. Hembree WC et al. Endocrine Treatment of Gender-Dysphoric/Gender-Incongruent Persons. J Clin Endocrinol Metab 2017;102(11):3869-3903. DOI:10.1210/jc.2017-01658
  3. Coleman E et al. Standards of Care for the Health of Transgender and Gender Diverse People, Version 8. Int J Transgend Health 2022;23(S1):S1-S259. DOI:10.1080/26895269.2022.2100644