Clinical Trial Details
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NCT02698384 : Therapeutic Strategies in Acromegalic Subjects Treated With Lanreotide 120mg
AgesMin: 18 Years Max: N/A
Inclusion Criteria:

- Male or female aged 18 years or more, suffering from acromegaly

- Treatment naïve or treated subject (whatever the previous treatments except
Lanreotide 120mg and radiotherapy) who does not achieve biochemical control in the
physician's opinion. Requiring a treatment with Somatostatin analog (SSA)

- Having performed a Magnetic Resonance Imaging (MRI) to evaluate the tumor size within
the previous 12 weeks (post-surgery MRI for operated subjects)

- In whom the physician has already decided to initiate a treatment with Lanreotide
120mg as a monotherapy

Exclusion Criteria:

- Subject previously/currently treated with Lanreotide 120mg

- History of radiotherapy for acromegaly

- Subject who requires a surgical intervention for relief of any sign or symptom
associated with tumor compression

- Concomitant prolactin hypersecretion requiring a treatment with dopaminergic agonists

- Active neoplastic disease
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