Table I.
Trial number | Phase | Line of treatment | Type of BTC | Estimated enrollment | Allocation | Study arms
|
Pathways targeted | Primary outcomes | Status | ||
---|---|---|---|---|---|---|---|---|---|---|---|
Arm A | Arm B | ||||||||||
Monotherapy | NCT04157985 | 3 | First-line | CCA | 578 | Randomized | Pembrolizumab or nivolumab or atezolizumab or ipilimumab or cemiplimab | N/A | PD-1/PD-L1 | Time to next treatment, PFS | Recruiting |
NCT03110328 | 2 | Second-line | CCA | 33 | N/A | Pembrolizumab | N/A | PD-1 | Best overall response, PFS, OS | Completed | |
NCT02054806 | 1b | Second- or later-line | CCA, GBC | 477 | N/A | Pembrolizumab | N/A | PD-1 | Best overall response | Completed | |
NCT02829918 | 2 | Second- or later-line | CCA, GBC | 54 | N/A | Nivolumab | N/A | PD-1 | ORR After 4 Cycles of Treatment | Active, not recruiting | |
NCT03999658 | 2 | Second- or later-line | CAA, GBC | 220 | Non-randomized | STI-3031 | N/A | PD-L1 | ORR | Not yet recruiting | |
NCT02628067 | 2 | Second- or later-line | CCA, GBC | 1,609 | Non-randomized | Pembrolizumab | N/A | PD-1 | ORR | Recruiting | |
NCT03201458 | 2 | Second- or later-line | CCA, GBC | 76 | Randomized | Atezolizumab | Atezolizumab plus cobimetinib | PD-L1, MEK1 | PFS | Active, not recruiting | |
NCT04238637 | 2 | Second- or later-line | ICC | 50 | Randomized | Durvalumab | Durvalumab plus tremelimumab | PD-L1, CTLA-4 | ORR | Recruiting | |
NCT04440943 | 1 | Second- or later-line | CCA | 40 | N/A | CDX-527 | N/A | PD-L1xCD27 | Safety, tolerability | Recruiting | |
NCT05101109 | 1 | Second- or later line | N/A | 36 | N/A | ABL501 | N/A | LAG-3xPD-L1 | Safety, tolerability | Recruiting | |
NCT03849469 | 1 | Second- or later-line | ICC | 242 | Non-Randomized | XmAb® 22841 | XmAb® 22841 plus pembrolizumab | CTLA-4xLAG-3, PD-1 | Safety, tolerability | Active, not recruiting | |
NCT03517488 | 1 | Second- or later-line | CCA | 154 | N/A | XmAb® 22842 | N/A | CTLA-4xLAG-3 | Safety, tolerability | Active, not recruiting | |
NCT03219268 | 1 | Second- or later-line | CCA | 353 N/A | Tebotelimab | Tebotelimab plus margetuximab | PD-1xLAG-3, HER2 | Safety, tolerability | Active, not recruiting | ||
NCT04802876 | 2 | N/A | CCA | 141N/A | Spartalizumab | N/A | PD-1 | ORR | Recruiting | ||
ICIs + chemotherapy | NCT04066491 | 2/3 | First line | CCA, GBC | 309 Randomized | M7824 plus GC GC | Placebo plus L1xTGF-β | PD- | Safety, OS recruiting | Active, not | |
NCT03046862 | 2 | First-line | CCA, GBC | 31 N/A | Durvalumab or tremelimumab plus GC | N/A | PD-L1, CTAL-4 | ORR | Active, not recruiting | ||
NCT03875235 | 3 | First-line | CCA, GBC | 810 Randomized | plus GC | Durvalumab GC | Placebo plus | PD-L1 | OS recruiting | Active, not | |
NCT04003636 | 3 | First-line | CCA, GBC | 1,048 Randomized | plus GC | Pembrolizumab GC | Placebo plus | PD-1 | OS recruiting | Active, not | |
NCT03260712 | 2 | First-line | CCA, GBC | 50 N/A | Pembrolizumab plus GC | N/A | PD-1 | PFS at 6 months | Active, not recruiting | ||
NCT03796429 | 2 | First-line | CCA, GBC | 40 N/A | Toripalimab plus GS | N/A | PD-1 | PFS, OS | Recruiting | ||
NCT04172402 | 2 | First-line | CCA, GBC | 48 N/A | Nivolumab plus GS | N/A | PD-1 | ORR | Active, not recruiting | ||
NCT04027764 | 2 | First-line | CCA, GBC | 30 N/A | Toripalimab plus S1 plus albumin paclitaxel | N/A | PD-1 | ORR | Recruiting | ||
NCT03478488 | 3 | First-line | CCA, GBC | 480 Randomized | GEMOX | KN035 plus | GEMOX | PD-L1 | OS | Recruiting | |
NCT03785873 | 1b/2 | Second-line | CCA, GBC | 34 N/A | Nivolumab plus 5-FU plus Nal-Irinotecan | N/A | PD-1 | Safety, tolerability, PFS | Active, not recruiting | ||
NCT03704480 | 2 | Second-line | CCA, GBC | 102 Randomized | plus tremelimumab | Durvalumab plus tremelimumab plus Paclitaxel | Durvalumab CTLA-4 | PD-L1, | PFS | Recruiting | |
NCT03111732 | 2 | Second- or later-line | CCA, GBC | 11 | N/A | Pembrolizumab plus oxaliplatin plus capecitabine | N/A | PD-1 | PFS | Completed | |
NCT03101566 | 2 | N/A | CCA, GBC | 75 | Randomized | Nivolumab plus GC | Nivolumab plus ipilimumab | PD-1, CTLA-4 | PFS at 6 months | Active, not recruiting | |
NCT04295317 | 2 | N/A | ICC | 65 | N/A | SHR-1210 plus capecitabine | N/A | PD-1 | RFS | Recruiting | |
NCT03311789 | 1/2 | N/A | CCA, | 30 | N/A GBC | Nivolumab or SHR-1210 plus GC | N/A | PD-1 | PFS at 6 months | Recruiting | |
ICIs + targeted therapy | NCT04361331 | 2 | First-line | ICC | 60 | Randomized | Toripalimab plus lenvatinib | Lenvatinib plus GEMOX | PD-1, TKI | ORR | Active, not recruiting |
NCT03895970 | 2b | Second-line | CCA, GBC | 50 | N/A | Pembrolizumab plus lenvatinib | N/A | PD-1, TKI | ORR, DCR, PFS | Recruiting | |
NCT02443324 | 1 | Second- or later-line | CCA, GBC | 298 | N/A | Pembrolizumab plus ramucirumab | N/A | PD-1, VEGFR-2 PD-1, | Safety, Tolerability | Completed | |
NCT05174650 | 2 | Second- or later-line | ICC | 37 | N/A | Atezolizumab plus derazantinib | N/A | FGFR1/2/3 | ORR | Recruiting | |
NCT04298021 | 2 | Second- or later-line | CCA, GBC | 74 | Non-Randomized | Durvalumab plus AZD6738 | AZD6738 + Olaparib | PD-L1, ATR/ATM, PARP | DCR | Recruiting | |
NCT03475953 | 1/2 | Second- or later-line | CCA, GBC | 482 | Non-Randomized | Avelumab plus regorafenib | N/A | PD-L1, TKI | RP2D, ORR | Recruiting | |
NCT04550624 | 2 | Second- or later-line | CCA, GBC | 40 | N/A | Pembrolizumab plus lenvatinib | N/A | PD-2, TKI | ORR | Recruiting | |
NCT04298008 | 2 | Third-line | CCA, GBC | 26 | N/A | Durvalumab + AZD6738 | N/A | PD-L1, ATR/ATM | DCR | Recruiting | |
NCT05010681 | 2 | N/A | ICC | 25 | N/A | Sintilimab plus lenvatinib | N/A | PD-1, TKI | ORR | Recruiting | |
NCT03639935 | 2 | Maintenance after first line platinum-based systemic chemo-therapy | CCA, GBC | 35 | N/A | Nivolumab plus rucaparib | N/A | PD-1, PARP | Proportion of patients alive and without radiological or clinical progression at 4 months | Recruiting | |
ICIs + Chemotherapy+ Target therapy | NCT04300959 | 2 | First-line | CCA, GBC | 80 | Randomized | Sintilimab plus anlotinib plus GC | N/A | PD-1, PDGFR, FGFR, VEGFR and c-KIT kinase | 12 months OS rate | Recruiting |
NCT05342194 | 3 | First-line | ICC | 480 | Randomized | Toripalimab plus lenvatinib plus GEMOX/GC | Placebo plus GEMOX/GC | PD-1, TKI | OS | Not yet recruiting | |
NCT03951597 | 2 | First-line | ICC | 30 | N/A | JS001 plus Lenvatinib plus GEMOX | N/A | PD-1, TKI | ORR | Active, not recruiting | |
NCT05211323 | 2 | First-line | ICC | 88 | Randomized | Atezolizumab plus bevacizumab plus GC | GC | PD-1, VEGFR | PFS | Recruiting | |
NCT04506281 | 2 | NAT | ICC | 128 | Randomized | Toripalimab plus lenvatinib plus GEMOX | Capecitabine | PD-1, TKI | Event-free survival | Recruiting | |
ICIs + other therapy | NCT03937895 | 1/2a | First-line | CCA, GBC | 40 | N/A | Pembrolizumab plus allogeneic natural killer cell | N/A | PD-1 | Safety, Tolerability, ORR | Completed |
NCT04866836 | 2 | Second | CCA, GBC | 20 | N/A | Tislelizumab plus radiotherapy | N/A | PD-1 | ORR | Recruiting | |
NCT04068194 | 1/2 | Second- or later-line | CCA, GBC | 39 | Randomized | Avelumab plus peposertib plus hypofractionated RT | Avelumab plus hypofractionated RT | PD-L1, DNA-PK | Safety, Tolerability, ORR | Recruiting | |
NCT05010668 | 2 | Second- or later-line | ICC | 25 | N/A | Sintilimab plus lenvatinib plus cryoablation | N/A | PD-1,TKI | ORR | Recruiting | |
NCT04299581 | 2 | Second- or later-line | ICC | 25 | N/A | Camrelizumab plus cryoablation | N/A | PD-1 | ORR | Recruiting | |
CAR-T | NCT03633773 | 1/2 | N/A | ICC | 9 | N/A | MUC-1 CART plus fludarabine plus cyclophosphamide | N/A | MUC-1 | DCR | Recruiting |
NCT04951141 | 1 | Second- or later-line | CCA | 10 | N/A | anti-GPC3 CAR-T | N/A | GPC3 | Safety | Recruiting | |
NCT05194735 | 1/2 | Second- or later-line | CCA | 180 | Non-randomized | TCR-T-cell drug product | TCR-T-cell drug product plus IL-2 | Neoantigens | Safety-ORR | Recruiting | |
Cancer vaccines | NCT04853017 | 1 | AT | CCA, GBC | 18 | N/A | ELI-002 2P Amph-CpG-7909 admixed with Amph modified KRAS peptides | N/A | KRAS | MTD, Safety | Recruiting |
NCT03942328 | 1 | N/A | CCA | 26 | N/A | EBRT, autologous DCs, pneumococcal 13-valent conjugate vaccine | N/A | Dendritic cells | Safety | Recruiting |
CCA, cholangiocarcinoma; BTC, biliary tract cancer; GBC, gallbladder cancer; PD-1, programmed cell death protein 1; PD-L1, programmed cell death ligand 1; CTLA-4, cytotoxic T-lymphocyte-associated antigen-4; LAG-3, lymphocyte-activation gene 3; DCR, disease control rate; 5-FU, 5-fluorouracil; GC, gemcitabine and cisplatin; GEMOX, gemcitabine and oxaliplatin; GS, gemcitabine and S-1; MTD, highest dose level for which >33% of subjects had a dose-limiting toxicity; N/A, not available; AT, adjuvant therapy; ORR, objective response rate; OS, overall survival; PFS, progression-free survival; RFS, recurrence-free survival; RP2D, recommended phase 2 dose; RT, radiotherapy.