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Surrogate Endpoints for Clinical Trials in Kidney Transplantation; Notice of Public Workshop; Correction

---
identifier: "/us/fr/2015-20832"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Surrogate Endpoints for Clinical Trials in Kidney Transplantation; Notice of Public Workshop; Correction"
title_number: 0
title_name: "Federal Register"
section_number: "2015-20832"
section_name: "Surrogate Endpoints for Clinical Trials in Kidney Transplantation; Notice of Public Workshop; Correction"
positive_law: false
currency: "2015-08-24"
last_updated: "2015-08-24"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "2015-20832"
document_type: "notice"
publication_date: "2015-08-24"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
fr_citation: "80 FR 51280"
fr_volume: 80
docket_ids:
  - "Docket No. FDA-2015-N-0001"
fr_action: "Notice; correction."
---

#  Surrogate Endpoints for Clinical Trials in Kidney Transplantation; Notice of Public Workshop; Correction

**AGENCY:**

Food and Drug Administration, HHS.

**ACTION:**

Notice; correction.

**SUMMARY:**

The Food and Drug Administration (FDA) is correcting a notice that appeared in the *Federal Register* of Monday, August 3, 2015 (80 FR 45999). The document announced a public workshop entitled “Surrogate Endpoints for Clinical Trials in Kidney Transplantation.” The document was published without the email address and fax number in the *Contact Person* section and without the option for email or phone registration in the *Registration* section. This document corrects those errors.

**FOR FURTHER INFORMATION CONTACT:**

Ramou Pratt, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 6193, Silver Spring, MD 20993-0002, 301-796-3928 or 301-796-1600, FAX: 301-595-7993, *[email protected].*

**SUPPLEMENTARY INFORMATION:**

In FR Doc. 2015-18911, appearing on page 45999 in the *Federal Register* of Monday, August 3, 2015, the following corrections are made:

1. On page 45999, in the first column, the *Contact Person* section is corrected to read: “ *Contact Person:* Ramou Pratt, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 6193, Silver Spring, MD 20993-0002, 301-796-3928 or 301-796-1600, FAX: 301-595-7993, *[email protected]* .”

2. On page 45999, in the second column, the *Registration* section is corrected to read: “ *Registration:* Email, fax, or phone your registration information (including name, title, firm name, address, telephone and fax numbers) to Ramou Pratt (see *Contact Person* ) by September 25, 2015. Registration is free for the public workshop. Early registration is recommended because seating is limited. Registration on the day of the public workshop will be provided on a space-available basis beginning at 8 a.m.

If you need special accommodations because of a disability, please contact Ramou Pratt (see *Contact Person* ) at least 7 days in advance.”

Dated: August 19, 2015.

Leslie Kux,

Associate Commissioner for Policy.