January 2026 SCRI Release Notes Copied

SCRI Trials and Trial Regimen Updates

The following updates were completed between December 12, 2025, and January 20, 2026. Sarah Cannon Research Institute now manages all SCRI/USOR trials and trial regimens.

For questions about these trials and regimens, please contact SCRIiKMEMRedits@McKesson.com.

New Builds Completed

Study Number Notes for New Build
25113 USOR 25113 BRE 474 Phase 3 Palazestrant or Placebo + Letrozole or Placebo + Ribociclib Q28D – v1.0 12Jun2025
25075 USOR 25075 GI 417 Phase 2 BMS-986504 or Placebo (400 mg) + Nab-paclitaxel + Gemcitabine Q28D – 24JUN2025

USOR 25075 GI 417 Phase 2 BMS-986504 or Placebo (600 mg) + Nab-paclitaxel + Gemcitabine Q28D – 24JUN2025

25030 USOR 25030 CLL 67 Phase 3 Arm A BGB-16673 Q28D – 13AUG2025

USOR 25030 CLL 67 Phase 3 Arm B Bendamustine + Rituximab Q28D – 13AUG2025

USOR 25030 CLL 67 Phase 3 Arm B Idelalisib + Rituximab Q28D – 13AUG2025

USOR 25030 CLL 67 Phase 3 Arm B Venetoclax + Rituximab Q28D – 13AUG2025

USOR 25030 CLL 67 Phase 3 Arm B Venetoclax Ramp-Up – 13AUG2025

24302 USOR 24302 GI 404 Phase 2 Arm A ONO-4578 + Opdivo + Bevacizumab + mFOLFOX6 Q28D – v3.0 20MAR2025

USOR 24302 GI 404 Phase 2 Arm B ONO-4578 + Opdivo + Bevacizumab + mFOLFOX6 Q28D – v3.0 20MAR2025

USOR 24302 GI 404 Phase 2 Arm C Bevacizumab + mFOLFOX6 Q28D – v3.0 20MAR2025

25007 USOR 25007 BRE 462 Phase 3 Arm 1 HER3-DXd Q84D – 25APR2025

USOR 25007 BRE 462 Phase 3 Arm 2 Capecitabine Q84D – 25APR2025

USOR 25007 BRE 462 Phase 3 Arm 2 Liposomal Doxorubicin Q84D – 25APR2025

USOR 25007 BRE 462 Phase 3 Arm 2 Nab-paclitaxel Q84D – 25APR2025

USOR 25007 BRE 462 Phase 3 Arm 2 Paclitaxel (80 mg/m2) Q84D – 25APR2025

USOR 25007 BRE 462 Phase 3 Arm 2 Paclitaxel (90 mg/m2) Q84D – 25APR2025

USOR 25007 BRE 462 Phase 3 Arm 2 T-DXd Q84D – 25APR2025

25131 USOR 25131 CML 30 Phase 3b Asciminib Q84D – v03 17MAY2024
24293 USOR 24293 GU 268 Phase 3 AAA817 + ARPI Q56D – v00 17JAN2025

USOR 24293 GU 268 Phase 3 AAA817 Q56D – v00 17JAN2025

USOR 24293 GU 268 Phase 3 ARPI Q56D – v00 17JAN2025

USOR 24293 GU 268 Phase 3 Cabazitaxel Q21D – v00 17JAN2025

USOR 24293 GU 268 Phase 3 Docetaxel Q21D – v00 17JAN2025

LUN 537
(ILCC)
LUN 537 Phase 3 V940 or Placebo + Pembrolizumab Q42D – 14Aug2025
25004 USOR 25004 AML 81 Phase 3 Intensive Therapy Consolidation Ziftomenib or Placebo + Cytarabine Q28D – 15AUG2025

USOR 25004 AML 81 Phase 3 Intensive Therapy Induction Ziftomenib or Placebo + Cytarabine + Daunorubicin Q28D – 15AUG2025

USOR 25004 AML 81 Phase 3 Maintenance Ziftomenib or Placebo Q28D – 15AUG2025

USOR 25004 AML 81 Phase 3 Nonintensive Therapy Ziftomenib or Placebo + Venetoclax + Azacitidine Q28D – 15AUG2025

25114 USOR 25114 GYN 162 Phase 2 INCB123667 Q28D – v3 15AUG2025
24221 USOR 24221 CH 03 Phase 3 Mavorixafor (X4P-001) or Placebo Q52W
25009 USOR 25009 LYM 256 Phase 2 Bridging Therapy (Placeholder) – v6.0 11MAR2025

USOR 25009 LYM 256 Phase 2 Cyclophosphamide + Fludarabine D-5,-4,-3 – v6.0 11MAR2025

USOR 25009 LYM 256 Phase 2 LYL314 D0 – v6.0 11MAR2025

25110 USOR 25110 GYN 161 Phase 2 Substudy 1 Bevacizumab Q21D – v3.0 22AUG2025

USOR 25110 GYN 161 Phase 2 Substudy 1 Mirvetuximab soravtansine + Bevacizumab Q21D – v3.0 22AUG2025

USOR 25110 GYN 161 Phase 2 Substudy 2 Mirvetuximab soravtansine + Carboplatin Q21D – v3.0 22AUG2025

25086 USOR 25086 RM 1145 Phase 1b GSK5764227 Q21D – 05MAR2025
25021 USOR 25021 BRE 466 Phase 3 Arm A PF-07248144 + Fulvestrant Q28D – 07APR2025

USOR 25021 BRE 466 Phase 3 Arm B Everolimus + Exemestane Q28D – 07APR2025

USOR 25021 BRE 466 Phase 3 Arm B Everolimus + Fulvestrant Q28D – 07APR2025

25154 USOR 25154 GI 428 Phase 2 Pumitamig or Bevacizumab + FOLFIRI Q14D – 09Oct2025

USOR 25154 GI 428 Phase 2 Pumitamig or Bevacizumab + FOLFOX Q14D – 09Oct2025

25173 USOR 25173 LUN 650 Phase 2 PF-08634404 + Carboplatin + Etoposide Q21D fb PF-08634404 Q21D – 06Nov2025
25174 USOR 25174 LUN 651 Phase 1b Part A PF-08634404 + Sigvotatug Vedotin Q42D – 23Oct2025

USOR 25174 LUN 651 Phase 1b Part B PF-08634404 + PF-08046054 Q21D – 23Oct2025

25139 USOR 25139 BRE 475 Phase 3 Part 1 Cohort 1 LY4064809 + Palbociclib + ET Q28D – 08Sep2025
25156 USOR 25156 LUN 645 Phase 3 Part 1 PF-08634404 or Placebo + Pembrolizumab or Placebo + Nab-paclitaxel + Carboplatin Q21D fb PF-08634404 or Placebo + Pembrolizumab or Placebo Q21D – 05Nov2025

USOR 25156 LUN 645 Phase 3 Part 1 PF-08634404 or Placebo + Pembrolizumab or Placebo + Paclitaxel + Carboplatin Q21D fb PF-08634404 or Placebo + Pembrolizumab or Placebo Q21D – 05Nov2025

USOR 25156 LUN 645 Phase 3 Part 2 PF-08634404 or Placebo + Pembrolizumab or Placebo + Pemetrexed + Carboplatin Q21D fb PF-08634404 or Placebo + Pembrolizumab or Placebo + Pemetrexed Q21D – 05Nov2025

24031 USOR 24031 GU 251 Phase 3 AAA817 Q56D – 18JUN2025

USOR 24031 GU 251 Phase 3 Standard of Care (Placeholder) – 18JUN2025

24325 USOR 24325 BRE 465 Phase 2 Arm A (1 or 2) Izalontamab Brengitecan Q21D – 30APR2025

USOR 24325 BRE 465 Phase 2 Arm B Capecitabine Q21D – 30APR2025

USOR 24325 BRE 465 Phase 2 Arm B Gemcitabine + Carboplatin Q21D – 30APR2025

USOR 24325 BRE 465 Phase 2 Arm B Nab-Paclitaxel Q28D – 30APR2025

USOR 24325 BRE 465 Phase 2 Arm B Paclitaxel Q28D – 30APR2025

24289 USOR 24289 LUN 589 Phase 3 Olomorasib or Placebo Q28D – 27JUN2025

USOR 24289 LUN 589 Phase 3 Part A Olomorasib or Placebo + Pembrolizumab Q21D – 27JUN2025

USOR 24289 LUN 589 Phase 3 Part B Olomorasib or Placebo + Durvalumab Q28D – 27JUN2025

24110 USOR 24110 LUN 605 Phase 2 Adjuvant Pembrolizumab Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 1 Neoadjuvant Pembrolizumab + Gemcitabine + Carboplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 1 Neoadjuvant Pembrolizumab + Gemcitabine + Cisplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 1 Neoadjuvant Pembrolizumab + Paclitaxel + Carboplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 1 Neoadjuvant Pembrolizumab + Paclitaxel + Cisplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 1 Neoadjuvant Pembrolizumab + Pemetrexed + Carboplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 1 Neoadjuvant Pembrolizumab + Pemetrexed + Cisplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 2 Adjuvant Gemcitabine + Carboplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 2 Adjuvant Gemcitabine + Cisplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 2 Adjuvant Paclitaxel + Carboplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 2 Adjuvant Pemetrexed + Carboplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 2 Adjuvant Pemetrexed + Cisplatin Q21D – 03JUL2025

USOR 24110 LUN 605 Phase 2 Arm 2 Neoadjuvant sac-TMT + Pembrolizumab Q21D – 03JUL2025

25070 USOR 25070 LUN 535 Phase 1b BBO-8520 + Pembrolizumab Q21D – v5.0 03SEP2025

USOR 25070 LUN 535 Phase 1b BBO-8520 Q21D – v5.0 03SEP2025

24270 USOR 24270 MDS 36 Phase 3 Azacitidine Q28D – v2.0 19SEP2024

USOR 24270 MDS 36 Phase 3 Ivosidenib Q28D – v2.0 19SEP2024

25116 USOR 25116 HN 43 Phase 3 Arm A Pembrolizumab + Carboplatin + Amivantamab Q21D – 23Jul2025

USOR 25116 HN 43 Phase 3 Arm B Pembrolizumab + Carboplatin + Fluorouracil Q21D – 23Jul2025

USOR 25116 HN 43 Phase 3 Arm B Pembrolizumab + Cisplatin + Fluorouracil Q21D – 23Jul2025

Updated Reference Information

Study Number Updated Reference Information Updated Drug Service Order Information Updated Regimen Instructions Other Changes
23094 PA10: 11 Apr 2025 (sponsor decision to hold pa9) N/A Regimen comments; Admin Update drug; instructions
23095 PAv5.0: 30 Jul 2025 N/A N/A Update drug; instructions
24093 Memo: 03 Oct 25 N/A N/A Update drug; instructions
24094 Site Edits: IPC Dispensation update N/A N/A Update drug; frequency
24234 PA 3.0; 04 August 2025 N/A N/A Update drug; instructions
22201 Update Drug Form to AIBW N/A N/A Update drug; dose/form
24310 Memo; 08 Sept 2025 N/A N/A Update drug; dose/form
24267 PM v5.0; 10th December 2025 N/A N/A Update drug; instructions, name
23284 PA 3.0, 18 June 2025 N/A Regimen comments; prophylaxis, observation Update drug; procurement
23289 Version 3.3; 5th August 2025 N/A N/A Update drug; instructions
24149 Version 4.0; 08 Sept 2025; V3.0;29Jul2025 N/A Regimen comments; admin, premedication Update drug; instructions
25018 Version 4.1; 24th November 2025 N/A N/A Update drug; instructions
24043 PA v3.0; 29 July 2025 N/A Regimen comments; Admin Update drug; premedication
24196 Version 3.0; 26 March 2025 N/A Regimen comments; admin, prophylaxis, premedication N/A
24070 Version 2.0; 05 November 2025 – PM v3.0; 06NOV2025 N/A Regimen comments; Observation Update drug; dose/form, instruction
24070 DIL; 21 November 2025 N/A N/A Update drug; instructions
24070 Memo; 18 November 2025 N/A N/A Update drug; instructions
24144 PM v8.0: 15 Oct 2025 N/A N/A Update drug; name and instructions
24006 PM v2.1: 09 Dec 2025 N/A N/A Update drug; instructions and name
23107 Version 5.0; 16 July 2025 N/A Regimen comments; admin Update drug; instructions
21270 PA v9.0: 03 Nov 2025 N/A Regimen comments; premedication Update drug; instructions
23234 PA v3.0; 13 May 2025 N/A Regimen comments; admin, premedication Update drug; admin/prep, instructions
23240 Version 8.0; 17 Sept 2025 N/A Regimen comments; admin Update drug; instructions
23085 PA v4.0; 20 June 2025 N/A N/A Update drug; instructions.

Added drug.