Search Legislation

Rare Cancers Act 2026

 Help about what version

What Version

 Help about advanced features

Advanced Features

 Help about opening options

Opening Options

Changes over time for: Rare Cancers Act 2026

 Help about opening options

Alternative versions:

Changes to legislation:

There are currently no known outstanding effects for the Rare Cancers Act 2026. Help about Changes to Legislation

Close

Changes to Legislation

Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.

Legislation Crest

Rare Cancers Act 2026

2026 CHAPTER 8

An Act to make provision to incentivise research and investment into the treatment of rare types of cancer; and for connected purposes.

[5th March 2026]

Be it enacted by the King’s most Excellent Majesty, by and with the advice and consent of the Lords Spiritual and Temporal, and Commons, in this present Parliament assembled, and by the authority of the same, as follows:—

1Review of law on marketing authorisationsU.K.

(1)The Secretary of State must—

(a)carry out a review of the law relating to marketing authorisations for orphan medicinal products that are for the diagnosis, prevention or treatment of cancer, and

(b)prepare and publish a report setting out the conclusions of the review.

(2)In carrying out the review the Secretary of State must, in particular, consider regulatory approaches in other countries.

(3)The report must be published before the end of the period of three years beginning with the day on which this Act is passed.

(4)The Secretary of State must lay a copy of the report before Parliament.

(5)In this section—

  • Human Medicines Regulations” means the Human Medicines Regulations 2012 (S.I. 2012/1916);

  • marketing authorisation” has the meaning given by section 9 of the Medicines and Medical Devices Act 2021;

  • medicinal product” has the meaning given by regulation 2 of the Human Medicines Regulations;

  • orphan medicinal product” means a medicinal product in relation to which the orphan criteria set out in regulation 50G(2) of the Human Medicines Regulations are met.

Commencement Information

I1S. 1 in force at 5.5.2026, see s. 5

2Secretary of State’s duties as to researchE+W

In section 1E of the National Health Service Act 2006 (Secretary of State’s duty to facilitate research etc)—

(a)the existing text becomes subsection (1);

(b)after that subsection insert—

(2)The research that the Secretary must facilitate or otherwise promote under subsection (1)(a) includes research into cancers that in the opinion of the Secretary of State are rare cancers.

(3)In discharging the duty under subsection (1)(a) in relation to those cancers, the Secretary of State must, in particular, ensure that there are such arrangements in place as the Secretary of State considers appropriate to—

(a)enable potential participants in clinical trials to be identified and contacted, and

(b)ensure that a person (to be known as “the National Specialty Lead for Rare Cancers”) is appointed with a job description that includes promoting and facilitating research into rare cancers by—

(i)providing advice in relation to the design and planning of research, and

(ii)facilitating collaboration between interested persons.

(4)In this section “rare cancer” means a cancer that affects not more than 1 in 2000 people in the United Kingdom.

Commencement Information

I2S. 2 in force at 5.5.2026, see s. 5

3Disclosure of information for research purposesE+W

(1)Section 261 of the Health and Social Care Act 2012 (power of NHS England to disclose information obtained in connection with information systems) is amended as follows.

(2)In subsection (5), after paragraph (d) insert—

(da)the disclosure is made for the purpose of facilitating the carrying out of relevant clinical trials (whether or not in the United Kingdom) by enabling potential participants in those trials to be identified and contacted,.

(3)After subsection (5) insert—

(5A)In subsection (5)(da)relevant clinical trials” means clinical trials in connection with the research and development of orphan medicinal products for the diagnosis, prevention or treatment of cancers that in the opinion of NHS England are rare cancers; and for this purpose—

(4)After subsection (6) insert—

(6A)A power conferred by this section to process information does not authorise the processing of information which would contravene the data protection legislation (but the power is to be taken into account in determining whether the processing would contravene that legislation).

(6B)In subsection (6A)the data protection legislation” and “processing” have the same meanings as in the Data Protection Act 2018 (see section 3 of that Act).

Commencement Information

I3S. 3 in force at 5.5.2026, see s. 5

4ExtentU.K.

(1)Sections 2 and 3 extend to England and Wales only.

(2)The remainder of this Act extends to England and Wales, Scotland and Northern Ireland.

Commencement Information

I4S. 4 in force at 5.5.2026, see s. 5

5CommencementU.K.

This Act comes into force at the end of the period of two months beginning with the day on which it is passed.

Commencement Information

I5S. 5 in force at 5.5.2026, see s. 5

6Short titleU.K.

This Act may be cited as the Rare Cancers Act 2026.

Commencement Information

I6S. 6 in force at 5.5.2026, see s. 5

Back to top

Options/Help

Print Options

Close

Legislation is available in different versions:

Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.

Original (As Enacted or Made): The original version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.

Close

See additional information alongside the content

Geographical Extent: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.

Show Timeline of Changes: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.

Close

Opening Options

Different options to open legislation in order to view more content on screen at once

Close

Explanatory Notes

Text created by the government department responsible for the subject matter of the Act to explain what the Act sets out to achieve and to make the Act accessible to readers who are not legally qualified. Explanatory Notes were introduced in 1999 and accompany all Public Acts except Appropriation, Consolidated Fund, Finance and Consolidation Acts.

Close

More Resources

Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as enacted version that was used for the print copy
  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • correction slips
  • links to related legislation and further information resources
Close

Timeline of Changes

This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.

Close

More Resources

Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as enacted version that was used for the print copy
  • correction slips

Click 'View More' or select 'More Resources' tab for additional information including:

  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • links to related legislation and further information resources