Pathways Study: Puberty Suppression

David Smith Excerpts
Monday 22nd June 2026

(1 month, 1 week ago)

Commons Chamber
Read Full debate Read Hansard Text Watch Debate Read Debate Ministerial Extracts
James Murray Portrait James Murray
- View Speech - Hansard - - - Excerpts

The hon. Lady refers, apparently with some certainty, to what she considers to be the clinical outcomes of these puberty blockers on young people. I have to say, with all due respect, that I would trust Dr Cass’s conclusion more than the hon. Lady’s, which is that there is not evidence about the risks or benefits of these medications. That is exactly why Dr Cass was so clear in recommending a trial to find that clinical evidence, because that is the basis on which we can take those decisions.

David Smith Portrait David Smith (North Northumberland) (Lab)
- View Speech - Hansard - -

I thank my right hon. Friend for his detailed and nuanced statement. Notwithstanding the risks of using puberty blockers on children, which he has outlined, and the inability to guarantee that they will not be harmed by participation in the trial, how can the trial determine long-term impacts of the use of puberty blockers when it lasts for only two years? Does that not show the inefficacy of the trial itself? If we really are committed to evidence, which I agree we should be, why are we not—as we just heard from the hon. Member for Reigate (Rebecca Paul)—using the long-term data that already exists, which came from clinics such as the Tavistock and was gathered over many years?

James Murray Portrait James Murray
- View Speech - Hansard - - - Excerpts

As a result of the work that the MHRA has been doing with these trial sponsors in recent months, there are now objective set criteria against which children and young people involved in the trial would be automatically withdrawn. Those criteria, as I set out earlier, will stop the short-term harm, and the view of the National Institute for Health and Care Research is that this means any long-term harm should not occur or go unnoticed. It is important that we ensure that the appropriate safeguards are in place for this trial. That is why I welcome what the MHRA has done in recent months, because it strengthens those safeguards, which are important in any clinical trial but, in this trial, could not be more important.