Pharmacokinetic Characterization of a Single 200 mg Dose of Doxycycline in Post-exposure Prophylaxis (PEP) of Sexually Transmitted Infections in Different Biological Compartments

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18-100
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Post-exposure prophylaxis (PEP) using doxycycline 200 mg within 24 hours of unprotected sexual intercourse to prevent sexually transmitted infections has demonstrated a reduction in the incidence of chlamydial and syphilis infections and syphilis infection by 70% and 73% in men who have sex with men (MSM) undergoing pre-exposure prophylaxis prophylaxis (PrEP) for HIV. Other studies are underway or in development on doxycycline prophylaxis for bacterial STIs, which are particularly common in this population. Monitoring adherence to PEP is of great interest in guaranteeing the effectiveness of this strategy and to be able to assess the uptake of PEP among PrEP users. Among the many methods for assessing adherence, measuring drug concentrations is a more accurate measure of adherence than self-reporting.

The therapeutic monitoring of doxycycline and the assessment of adherence have been described using plasma and hair samples, allowing estimation of intake over the last 3-4 days and 4 months, respectively. Nevertheless, these biological matrices present several limitations for application in clinical practice: reflecting the duration of exposure should be more in line with the frequency of visits (2 months), and the collection of hair samples may be difficult due to refusal or short hair. On the other hand, interpretation of the hair assay is limited by the degradation of doxycycline in this matrix, which could lead to underestimation of drug intake. By Therefore, new biological matrices are needed for more accurate assessment of doxycycline adherence in post-exposure prevention monitoring.

The objective is to evaluate the pharmacokinetics of doxycycline in plasma, whole blood, dried blood spots (DBS), urine and hair after a single dose of doxycycline in men using oral doxycycline for post-exposure prophylaxis of sexually transmitted infections (syphilis or Chlamydia trachomatis) and having sex with men.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult male patient

Men who have Sex with Men (MSM) on PrEP or HIV-infected patients

Patients who have not taken doxycycline for at least 3 months

No symptoms of bacterial STI infection (chlamydia, gonorrhea, Mycoplasma genitalium or syphilis).

Disqualifiers

Systemic treatment with retinoids (Acnetrait®, Procuta®, Curacné®, Contracné®, ....).

Treatment with enzyme-inducing anticonvulsants (carbamazepine, phenobarbital, phenytoin, etc.).

Known allergy to antibiotics of the tetracycline family.

Known allergy to one of the components of doxycycline tablets.

Trial design

Design model

Single group

Treatments tested in this trial

  • Samples

    Other intervention

    Blood samples, urine samples and oropharyngeal swabs before taking 200mg of doxycycline and then 2h, 24h, 48h, 7 days, 14 days, 60 days and 90 days after the single dose of doxycycline Hair samples: at the time of doxycycline administration, 1 month and 3 months after the single dose of doxycycline

Treatment groups

25 Participants
are divided into 1 treatment group
Group A: Adult male patientOther 1 intervention

Trial outcomes

Primary outcomes

1

Concentration of doxycycline in urine

Time frame
At Day 90

Secondary outcomes

1

Concentration of doxycycline in plasma

Time frame
Before the single intake of doxycycline
2

Concentration of doxycycline in plasma

Time frame
2 hours after doxycycline intake
3

Concentration of doxycycline in plasma

Time frame
24 hours after doxycycline intake
4

Concentration of doxycycline in plasma

Time frame
48 hours after doxycycline intake

Other outcomes

Sponsors and contacts

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